A Pilot Functional Performances Study of Two Synthetic Male Condom

Functional Performance Clinical Trial

— WONDALEAF-MEN  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03324594
• Other study ID #: NMRR-17-1895-37590
• Status: Completed
• Phase: N/A
• Start date: November 1, 2017
• Est. completion date: March 31, 2018

Study information

• Verified date: July 2018
• Source: Clinical Research Centre, Malaysia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: March 31, 2018
• Est. primary completion date: March 31, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Their female sexual partners are not at risk of pregnancy (using alternate contraception);

2. They don't have known sexually transmitted infections, including HIV/AIDS;

3. They should be experienced condom users, minimum 10 male condoms used in the last 12 months;

4. They are between 18 to 45 years of age;

5. They are in a monogamous heterosexual relationship and agree to practice vaginal sex only using male condoms provided by the study.

Exclusion Criteria:

1. couples who work for the research team or who are close relatives of the research team;

2. men with known allergy to natural rubber latex;

3. men with known sensitivity to the residual chemicals used in the manufacture of natural rubber latex condoms or the test condom materials;

4. couples where one knowingly has a sexually transmitted infection.

5. couples who are pregnant in time of recruitment

Related Conditions & MeSH terms

• Functional Performance
• Synthetic Male Condom

Intervention

Device:
• (1) WONDALEAF-CAP, (2) WONDALEAF-ON-MEN, (3) durex-TOGETHER (active comparator)
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.

Locations

Country	Name	City	State
Malaysia	Sarawak Family Planning Association	Kuching	Sarawak
Malaysia	Sarawak Research Society	Kuching	Sarawak

Sponsors (3)

Lead Sponsor	Collaborator
Clinical Research Centre, Malaysia	Sarawak Research Society, Twin Catalyst Sdn. Bhd.

Country where clinical trial is conducted

Malaysia, 

References & Publications (5)

Bounds W, Molloy S, Guillebaud J. Pilot study of short-term acceptability and breakage and slippage rates for the loose-fitting polyurethane male condom eZ.on bi-directional: a randomized cross-over trial. Eur J Contracept Reprod Health Care. 2002 Jun;7(2):71-8. — View Citation

Duarte JT, de Almeida AE, de Mello Pereira Abrantes S. Quality evaluation of commercially available male condoms in Rio de Janeiro, Brazil, 2009-2011. Reprod Health. 2016 Dec 7;13(1):145. — View Citation

Fontanet AL, Saba J, Chandelying V, Sakondhavat C, Bhiraleus P, Rugpao S, Chongsomchai C, Kiriwat O, Tovanabutra S, Dally L, Lange JM, Rojanapithayakorn W. Protection against sexually transmitted diseases by granting sex workers in Thailand the choice of using the male or female condom: results from a randomized controlled trial. AIDS. 1998 Oct 1;12(14):1851-9. — View Citation

French PP, Latka M, Gollub EL, Rogers C, Hoover DR, Stein ZA. Use-effectiveness of the female versus male condom in preventing sexually transmitted disease in women. Sex Transm Dis. 2003 May;30(5):433-9. — View Citation

Gallo MF, Grimes DA, Lopez LM, Schulz KF. Non-latex versus latex male condoms for contraception. Cochrane Database Syst Rev. 2006 Jan 25;(1):CD003550. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical Slippage Rates (CSR)	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.	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
Primary	Clinical Breakage Rates (CBR)	Number of condoms that broke during intercourse or withdrawal, divided by the number of condoms used during intercourse; reported as a percentage.	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
Primary	Clinical Failure Rates (CFR)	CFR is the sum of CSR and CBR for each condom type	Through study completion, an average of 3 months. In specific, CFR will be calculated after completion of four times usage, for each condom type
Secondary	Incidence of Treatment-Emergent Adverse Events	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.	Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type
Secondary	Comfort in use	This will reflect the acceptability of the male condoms used. It is a self-reported comfortability on each type of male condoms used	Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type
Secondary	Ease of insertion and removal	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	Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type
Secondary	Favorability of product attributes	This will reflect the acceptability of the male condoms used. It is a self-reported favorability towards attributes of each male condoms' type used	Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type
Secondary	Adequacy and feel of lubrication	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.	Through study completion, an average of 3 months. In specific, it will be measured after completion of four times usage, for each condom type

External Links

•   ISO/WD 29943-1. Condoms — Guidance on clinical studies — Part 1: Male condoms, clinical function studies based on self-reports