NCT Number: NCT04332120
Comparison of Results of Different Surgical Techniques Used in Female Tubal Sterilization
The investigator's aim in this study is to compare the results of tubal ligation surgery, one of the contraceptive methods, between different surgical techniques. 194 patients were included in the study. Of these patients, 104 had vaginal approach, 44 had laparotomic and 46 had laparoscopic tube ligation surgery. These surgical techniques are statistically was compared; Visual Analog Pain Scale (VAS) after surgery, in terms of duration of surgery, length of hospital stay, cost to hospital and amount of blood loss. As a result of the analysis; tubal sterilization technique performed with vaginal colpotomy were found to be more successful than other techniques; Visual Analog Pain Scale score, postoperative hospital stay, operation time and cost.
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Notify MeKey information
Conditions
Age range
32 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
About this study
The study compared the peroperative effects and postoperative results of different surgical techniques with three different techniques in patients undergoing tubal sterilization.
surgical techniques used:
- Mini Laparotomic tubal ligation
- Laparoscopic tubal ligation
- tubal ligation by posterior colpotomy
A total of 194 patients were included in the study. Tubal ligation was performed in 44 patients with mini laparotomy, 46 patients with laparoscopy and 104 patients with posterior colpotomy technique.
The following parameters were evaluated in the study
- Parity
- How many of their previous births are vaginal delivery, how many are cesarian section
- 6th hour Visual Analog Pain Scale (VAS) score
- 24th hour Visual Analog Pain Scale (VAS) score
- Preoperative - postoperative hmg differences
- Surgery time
- Length of hospital stay
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Over 31 years old
- Have completed the fertility request
- Accepting informed consent
Exclusion criteria
- Being under the age of 32
- Having a child desire
Treatment and study plan
Primary outcomes
-
Visual Analog Pain Scale (VAS)
Time frame: postoperative 6th hour
postoperative pain degree. 0-10 point. 0 worst, 10 best
-
Visual Analog Pain Scale (VAS)
Time frame: postoperative 24th hour
postoperative pain degree. 0-10 point. 0 worst, 10 best
-
the amount of bleeding
Time frame: 24 hour
preoperative and postoperative hemogram differences
-
length of hospital stay
Time frame: 48 hour
postoperative hospitalization
-
duration of surgery
Time frame: minimum duration of surgery 15 minute, maximum duration of surgery 60 minute
The time from the administration of anesthesia to the end of the operation
Sponsors and collaborators
Lead sponsor
Alanya Alaaddin Keykubat University
Other
Registry information
Important dates
- Study start
- 2016
- Primary completion
- 2018
- Study completion
- 2020
- First posted
- Apr 2, 2020
- Registry last updated
- Apr 2, 2020
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.
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