A Pilot Functional Performances Study of Two Synthetic Male Condom
- Conditions
- Synthetic Male CondomFunctional Performance
- Interventions
- Device: (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator)
- Registration Number
- NCT03324594
- Lead Sponsor
- Clinical Research Centre, Malaysia
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 50
- 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.
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Group E (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator) Participants will be first given (1) durex-TOGETHER, followed by (2) WONDALEAF-ON-MEN, and last with (3) WONDALEAF-CAP after completion of four times usage for each condom type. The participants will be asked to complete four times of usage for each condom type within three to four months. There will be a baseline survey before the use of the first condom type, and subsequent evaluations upon completion of each condom type. Group A (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator) Participants will be first given (1) WONDALEAF-CAP, followed by (2) WONDALEAF-ON-MEN, and last with (3) durex-TOGETHER after completion of four times usage for each condom type. The participants will be asked to complete four times of usage for each condom type within three to four months. There will be a baseline survey before the use of the first condom type, and subsequent evaluations upon completion of each condom type. Group C (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator) Participants will be first given (1) WONDALEAF-ON-MEN, followed by (2) durex-TOGETHER, and last with (3) WONDALEAF-CAP after completion of four times usage for each condom type. The participants will be asked to complete four times of usage for each condom type within three to four months. There will be a baseline survey before the use of the first condom type, and subsequent evaluations upon completion of each condom type. Group D (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator) Participants will be first given (1) WONDALEAF-ON-MEN, followed by (2) WONDALEAF-CAP, and last with (3) durex-TOGETHER after completion of four times usage for each condom type. The participants will be asked to complete four times of usage for each condom type within three to four months. There will be a baseline survey before the use of the first condom type, and subsequent evaluations upon completion of each condom type. Group B (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator) Participants will be first given (1) WONDALEAF-CAP, followed by (2) durex-TOGETHER, and last with (3) WONDALEAF-ON-MEN after completion of four times usage for each condom type. The participants will be asked to complete four times of usage for each condom type within three to four months. There will be a baseline survey before the use of the first condom type, and subsequent evaluations upon completion of each condom type. Group F (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator) Participants will be first given (1) durex-TOGETHER, followed by (2) WONDALEAF-CAP, and last with (3) WONDALEAF-ON-MEN after completion of four times usage for each condom type. The participants will be asked to complete four times of usage for each condom type within three to four months. There will be a baseline survey before the use of the first condom type, and subsequent evaluations upon completion of each condom type.
- Primary Outcome Measures
Name Time Method Clinical Slippage Rates (CSR) 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.
Clinical Breakage Rates (CBR) 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.
Clinical Failure Rates (CFR) 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 Outcome Measures
Name Time Method Adequacy and feel of lubrication 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.
Incidence of Treatment-Emergent Adverse Events 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.
Comfort in use 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
Favorability of product attributes 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
Ease of insertion and removal 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
Trial Locations
- Locations (2)
Sarawak Family Planning Association
🇲🇾Kuching, Sarawak, Malaysia
Sarawak Research Society
🇲🇾Kuching, Sarawak, Malaysia