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Completed

NCT Number: NCT03324594

A Pilot Functional Performances Study of Two Synthetic Male Condom

Over the decades, male condoms had been widely commercialized and used to protect against unintended pregnancy and sexually transmitted infections (STI). While natural rubber latex (NRL) male condoms has majority proportion of male condoms in the market, synthetic male condoms (SMC) made from polyurethane or other synthetic materials remain new to the consumers. Notably, synthetic male condoms are found to be more durable, non-allergenic and have better compatibility with lubricants when compared to NRL male condoms. The SMCs that have FDA approval and commercially available are AvantiTM (polyisoprene condom), Trojan SupraTM (polyurethane condom) and eZ.onTM (polyurethane condom). Although the effectiveness of SMCs in the prevention of sexually transmitted infections has yet to be established, SMCs are believed to be comparable to NRL male condoms in both STI prevention and contraception protection. Notwithstanding, a recent literature had reported the shortfall on the quality of variant male condoms in the market, especially nonconforming volumetric capacity, burst pressure and freedom from holes. This warrant the current investigation, to evaluate the functional performances of two newly invented synthetic male condoms, branded as "WONDALEAF-CAP" (WLC) and "WONDALEAF-ON-MAN" (WLM). Apart from being made of polyurethane, the major feature of WLC and WLM are nonetheless their adhesive coating on the outer rim of the condom opening which by securely adhering to the foreskin, prevent slippage of condom and spillage of male ejaculate or secretions when the penis is flaccid, and thereby improve the user-friendliness of condom usage.

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Key information

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Sarawak Family Planning Association, Kuching, Sarawak, Malaysia

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Their female sexual partners are not at risk of pregnancy (using alternate contraception);
  • They don't have known sexually transmitted infections, including HIV/AIDS;
  • They should be experienced condom users, minimum 10 male condoms used in the last 12 months;
  • They are between 18 to 45 years of age;
  • They are in a monogamous heterosexual relationship and agree to practice vaginal sex only using male condoms provided by the study.

Exclusion criteria

  • couples who work for the research team or who are close relatives of the research team;
  • men with known allergy to natural rubber latex;
  • men with known sensitivity to the residual chemicals used in the manufacture of natural rubber latex condoms or the test condom materials;
  • couples where one knowingly has a sexually transmitted infection.
  • couples who are pregnant in time of recruitment

Treatment and study plan

(1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator)

Device
  • WONDALEAF-ON-MEN (WLM) is a polyurethane pouch with outstretching adhesive shield. The pouch covers the penis in man user; while the adhesive shield covers the groin regions to provide extra protection for the couples. The pouch is equivalent to marketed polyurethane male; while the adhesive shield is equivalent to marketed polyurethane wound dressing. WLM integrally joined with an adhesive wound dressing, both made of the same polyurethane material.
  • WONDALEAF-CAP (WLC) is a miniature form of WLM: the pouch covers glans penis and the adhesive shield wraps around the shaft of the penis only, thereby emulating the configuration of a donned regular condom on the penis. Because of the adhesive coating, WLC overcomes the problems of slippage when the penis is flaccid.
  • The durex-TOGETHER serves as the active comparator in this study. It is a transparent natural rubber latex male condom which is commercially available.

Primary outcomes

  1. Clinical Slippage Rates (CSR)

    Time frame: Through study completion, an average of 3 months. In specific, CSR will be evaluated within 24 hours after use of individual condom, for each condom type

    Number of condoms that slipped completely off the penis during intercourse or withdrawal, divided by the number of condoms used during intercourse; reported as a percentage.

  2. Clinical Breakage Rates (CBR)

    Time frame: Through study completion, an average of 3 months. In specific, CBR will be evaluated within 24 hours after use of individual condom, for each condom type

    Number of condoms that broke during intercourse or withdrawal, divided by the number of condoms used during intercourse; reported as a percentage.

  3. Clinical Failure Rates (CFR)

    Time frame: Through study completion, an average of 3 months. In specific, CFR will be calculated after completion of four times usage, for each condom type

    CFR is the sum of CSR and CBR for each condom type

Secondary outcomes

  1. Incidence of Treatment-Emergent Adverse Events

    Time frame: Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type

    This outcome will reflect the safety of the male condoms used. Proportion of participants with symptoms of and proportion of condom uses with reports of individual complaints (eg. irritation, burning, itching, bleeding, etc.) during or immediately after any of the 3 separate uses will be calculated for each condom type. Adverse events will be classified by relatedness, expectedness and severity.

  2. Comfort in use

    Time frame: Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type

    This will reflect the acceptability of the male condoms used. It is a self-reported comfortability on each type of male condoms used

  3. Ease of insertion and removal

    Time frame: Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type

    This will reflect the acceptability of the male condoms used. It is a self-reported ease of insertion and removal for each type of male condoms used

  4. Favorability of product attributes

    Time frame: Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type

    This will reflect the acceptability of the male condoms used. It is a self-reported favorability towards attributes of each male condoms' type used

  5. Adequacy and feel of lubrication

    Time frame: Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type

    This will reflect the acceptability of the male condoms used. It is a self-reported adequacy and feel of lubrication for each type of male condoms used.

Sponsors and collaborators

Lead sponsor

Clinical Research Centre, Malaysia

Other

Collaborators

  • Sarawak Research Society
  • Twin Catalyst Sdn. Bhd.

Registry information

Official study title

A Pilot Functional Performances Study of The Wondaleaf-Cap and The Wondaleaf-On-Man Synthetic Male Condom

Acronym: WONDALEAF-MEN

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Oct 27, 2017
Registry last updated
Jul 18, 2018

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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