Clinica Profamilia
Santo Domingo, 10401, Dominican Republic
Completed
NCT Number: NCT01283555
Comparative Safety Study of Two Vaginal Applicators With Tenofovir
The primary objective of this study is to compare the effect of two vaginal applicators, delivering the candidate microbicide Tenofovir, on symptoms and signs of irritation of the external genitalia, cervix and vagina as seen on colposcopy after seven days of twice daily use.
The secondary objectives are to:
1. Evaluate and compare the dosing accuracy and precision of the user-filled applicator and pre-filled applicator with the candidate microbicide, Tenofovir. 2. Compare the acceptability of the user-filled applicator with the pre-filled applicator.
Completed
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Conditions
Age range
18 year–50 year
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Female
- Age 18 to 50, inclusive
- Pre-menopausal
- In good health as reported by individual
- Have regular menstrual cycles (24 to 35 days)
- Low risk for sexually transmitted infections (only one sexual partner in the last three months)
- Not pregnant or at risk of pregnancy (must either have had a tubal ligation, or currently be using a hormonal method of contraception)
- Negative on a urine pregnancy test
- Willing to abstain from sexual intercourse and masturbation during two 7-day periods when applicators are being used
- Willing to abstain from use of vaginal products during course of study (including douching, use of vaginal applicators for medication, lubrication, sex toys, other)
- Willing to follow procedural requirements of study
- Willing and able to provide informed consent for study participation
- Willing to provide investigator with phone number or address where she can be reached during the study
Exclusion criteria
- History of hysterectomy
- Pregnancy or within two months of last pregnancy outcome (delivery, spontaneous or induced abortion, medical or surgical management of ectopic pregnancy)
- Post-menopausal
- Breastfeeding
- Use of an intra-uterine device (IUD), cervical caps or diaphragm for contraceptive purposes
- Diagnosis or treatment for a sexually transmitted disease within the past 30 days;
- More than one sexual partner in the last 3 months
- Has had surgery on the external genitalia, vagina, or cervix within the past 3 months;
- Current or past use of any anti-retroviral therapies including but not limited to systemic Tenofovir (Viread®)
- Current or anticipated use of drugs on a daily basis that may reduce renal function (e.g. acyclovir or ibuprofen) or liver function (e.g. Tylenol)
- HIV positive at time of screening
- Hepatitis B surface antigen (HBsAg) positive at time of screening
- Positive test results for Neisseria gonorrhea, Chlamydia trachomatis, or Trichomonas vaginalis at time of screening.
- At baseline colposcopic exam (Visit 2), findings involving disruption of epithelium with disruption of blood vessels or deep disruption of epithelium alone. Any area of epithelium with bleeding will be considered deeply disrupted.
- Any abnormal finding on colposcopic exams which in the opinion of the investigator, precludes participation in the study
- At baseline exams, clinical symptoms or signs of vaginitis or vulvitis confirmed by a wet mount exam of the discharge. Note: If vaginitis or vulvitis is present at either baseline exam (visits 2 or 10), volunteer will be treated and rescheduled for new baseline exam one week after application of last treatment dose. If signs or symptoms are still present at the rescheduled baseline exam for Visit 2, the volunteer will not be enrolled into study. If signs or symptoms are still present at the rescheduled baseline exam for Visit 10, the volunteer will be discontinued from the study.
- Serum chemistry (glucose, creatinine, bilirubin, AST [aspartate aminotransferase] and ALT [alanine transaminase]) not within normal expected levels according to the specifications of the local laboratory.
- Hemoglobin, hematocrit and total white blood cell not within 15 % of lower and upper limit normal levels according to the specifications of the local laboratory.
- Participation in any other research study in the 30 days prior to screening and/or plans to participate in any other research study during the entire study duration.
Treatment and study plan
Tenofovir
DrugDelivered using prefilled and user-filled applicator
Other names: TFV
Primary outcomes
-
Number of Colposcopic Findings (Baseline and After One Week of Product Use)
Time frame: 7 days
Comparison of colposcopic findings between baseline visits and after one week of twice-daily application of Tenofovir 1% gel with either a user-filled or prefilled applicator
Secondary outcomes
-
Filled Volume
Time frame: 3 dose delivery measurements during 1 week of product use
At each dose delivery visit, the applicator was weighed, prior to vaginal insertion. For the user-filled applicator, the participant handed the applicator to the investigator after filling with gel from the multidose tube. The applicator was then weighed and returned to the participant for insertion. For the prefilled applicator, the participant inserted the plunger into the barrel, and then handed the applicator to the investigator for weighing.
-
Filling Precision (5% Range)
Time frame: 3 dose delivery measurements during 1 week of product use
A 5% range was calculated around the average filled volumes to determine how many applicators were filled within this range (+/-5% of average volume)
-
Filling Precision (10% Range)
Time frame: 3 dose delivery measurements during 1 week of product use
A 10% range was calculated around the average filled volumes to determine how many applicators were filled within this range (+/-10% of average volume)
-
Filling Accuracy (% of Target Dose)
Time frame: 3 dose delivery measurements during 1 week of product use
The target dose for Tenofovir gel in this study was 4.0ml, which is the volume of Tenofovir being used in current microbicide clinical trials. The filled volume for each applicator was compared with the intended target dose of 4.0ml.
-
Dosing Volume (Expressed Volume)
Time frame: 3 dose delivery measurements during 1 week of product use
At each dose delivery visit, the applicator was weighed prior to vaginal insertion and after use. The volume of gel expressed was measured using the following data: weight of filled applicator, weight of emptied applicator, the average weight of an empty applicator, and gel density.
-
Dosing Precision, 5% (Expressed Volume)
Time frame: 3 dose delivery measurements during 1 week of product use
A 5% range was calculated around the average expressed volume of 3.83ml to determine how many applicators delivered a dose within this range (+/-5% of average volume)
-
Dosing Precision, 10% (Expressed Volume)
Time frame: 3 dose delivery measurements during 1 week of product use
A 10% range was calculated around the average expressed volume of 3.83ml to determine how many applicators delivered a dose within this range (+/-10% of average volume)
-
Dosing Accuracy (% of Target Dose Delivered)
Time frame: 3 dose delivery measurements during 1 week of product use
The target dose for Tenofovir gel in this study was 4.0ml, which is the volume of Tenofovir being used in current microbicide clinical trials. The average dose delivered for each applicator was compared with the intended target dose of 4.0ml.
-
Number of Participants Reporting Applicator Easy to Fill
Time frame: Final study visit (after completing both study arms)
Participants were asked to describe the process of filling the user-filled applicator.
Response categories included "easy", "moderately difficult", and "difficult".
Since "ease of filling" only applies to the user-filled applicator, this question was not applicable for the prefilled applicator.
-
Number of Respondents Reporting Confidence With Filling the User-filled Applicator
Time frame: Final study visit (after completing both study arms)
Participants were asked when using the user-filled applicator, how confident did they feel that they at inserted the correct amount of gel into the applicator.
Response categories included "very confident", "confident", and "not confident".
(Note: this question does not apply to the prefilled applicator.)
-
Reasons Given by Participants for Knowing When the Applicator Was Filled Correctly
Time frame: Final study visit (after completing both study arms)
Participants were asked how did they know when the applicator was filled correctly (that is, with the right amount of gel). More than one answer was allowed.
Response categories included "plunger automatically stopped", "the 'FULL' line was reached", and "other".
Note: this question does not apply to the prefilled applicator.
-
Number of Participants Reporting Applicator Easy to Insert
Time frame: Final study visit (after completing both study arms)
Participants were asked to describe the insertion of the applicator into the vagina for each applicator (user-filled and prefilled).
Response categories included "easy", "moderately difficult", and "difficult".
-
Number of Participants Reporting That the Gel Was Easy to Dispense
Time frame: Final study visit (after completing both study arms)
Participants were asked to describe the dispensing of the gel into the vagina with each applicator (user-filled and prefilled).
Response categories included "easy", "moderately difficult", and "difficult".
-
Number of Participants Reporting Applicator Preference (User-filled or Prefilled) Across a Variety of Factors
Time frame: Final study visit (after completing both study arms)
Participants were asked about their preference for either the user-filled or prefilled applicator with regard to several use factors as well as in relation to disposal, storage, and overall comfort and preference.
Response categories included "user-filled", "prefilled", and "same".
-
Number of Participants Reporting That Applicator Was Comfortable to Use
Time frame: Final study visit (after completing both study arms)
Participants were asked to describe the comfort of use for each applicator type(user-filled and prefilled).
Response categories included "comfortable", "neutral", and "uncomfortable".
-
Number of Participants Reporting Suggestions Regarding Ease of Use or Comfort
Time frame: Final study visit (after completing both study arms)
Participants were asked if they could suggest ways that would make each applicator easier or more comfortable to use. Response categories were "yes" and "no". If yes, participants were asked to describe how they would make the applicator easier and/or more comfortable to use.
-
Number of Participants Reporting That the Instructions for Use Were Helpful
Time frame: Final study visit (after completing both study arms)
For each applicator type, participants were asked if the instructions were helpful to you.
Response categories were "yes" and "no".
-
Number of Participants Reporting That Both Applicators Were Acceptable
Time frame: Final study visit (after completing both study arms)
Participants were asked if both applicators were acceptable to them. Responses were either "yes" or "no".
-
Number of Participants Reporting That the Cost of the Applicator Would Influence Their Choice of Applicator
Time frame: Final study visit (after completing both study arms)
Participants were asked if the cost of the applicator would influence their choice of applicator.
Response categories were "yes", "no", and "maybe".
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Number of Participants Reporting That They Would Use the User-filled Applicator in the Future if it Came With a Gel for HIV Prevention
Time frame: Final study visit (after completing both study arms)
Participants were asked if they would use the user-filled applicator in the future if it came with a gel that helped prevent HIV infection.
Response categories included "yes", "no", and "in some circumstances".
-
Number of Participants Reporting That They Would Not Want to Use the User-filled Applicator in the Future if it Came With a Gel for HIV Prevention
Time frame: Final study visit (after completing both study arms)
Participants were asked if there were any reasons that they would not want to use this user-filled applicator in the future if it came with a gel that helped prevent HIV infection.
Response categories included "yes", "no", and "in some circumstances".
-
Number of Participants Reporting That They Would Recommend the User-filled Applicator for HIV Prevention
Time frame: Final study visit (after completing both study arms)
Participants were asked if they would recommend the user-filled applicator to other women if it came with a gel that helped prevent HIV infection.
Response categories included "yes", "no", and "in some circumstances".
Sponsors and collaborators
Lead sponsor
PATH
Other
Collaborators
- CONRAD
- Profamilia, Santo Domingo, DR
Registry information
Official study title
Comparative Safety Study of Pre-Filled Plastic and User-Filled Paper Vaginal Applicators With Candidate Microbicide, Tenofovir
Important dates
- Study start
- 2011
- Primary completion
- 2011
- Study completion
- 2011
- First posted
- Jan 26, 2011
- Registry last updated
- Jul 16, 2012
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.