Circumcision, Male Clinical Trial
— Unicirc004Official title:
Adult Male Circumcision With Unicirc Under Topical Anesthetic vs Open Surgical Circumcision: a Randomized Controlled Trial
Verified date | September 2018 |
Source | Simunye Primary Health Care |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
RCT of Unicirc under topical anesthetic w/ cyanoacrylate wound sealing vs. open surgical circumcision under local anesthetic with suturing.
Status | Completed |
Enrollment | 75 |
Est. completion date | September 2015 |
Est. primary completion date | September 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Healthy male - Uncircumcised - With normal penile anatomy Exclusion Criteria: - Concurrent illness - History of bleeding disorder - Past reaction to local anesthetic - Infection - Penile abnormality which could complicate circumcision |
Country | Name | City | State |
---|---|---|---|
South Africa | Lonmin Hospital | Marikana | Northwest |
Lead Sponsor | Collaborator |
---|---|
Simunye Primary Health Care |
South Africa,
Millard PS, Goldstuck ND. No-needle, single-visit adult male circumcision with Unicirc: a multi-centre field trial. PLoS One. 2015 Mar 30;10(3):e0121686. doi: 10.1371/journal.pone.0121686. eCollection 2015. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time Elapsed From First Clamp (Surgical) or Start of Insertion of Bell (Unicirc) to Beginning of Wound Dressing | Time elapsed from first clamp (surgical) or start of insertion of bell (Unicirc) to beginning of wound dressing | Up to 30 minutes | |
Secondary | Surgical Pain 0=no Pain; 10=Worst Pain Ever | Self-described pain severity during procedure (scale 1 to 10). 0=no pain, 5=moderate pain, 10=worst pain ever | Up to 30 minutes | |
Secondary | Completely Healed at 4 Weeks | Number of participants who were completely healed at 4 weeks | At the 4-week followup visit | |
Secondary | Wound Dehiscence | Proportion experiencing wound dehiscence (< 2 cm vs > 2 cm) | Up to 4 weeks | |
Secondary | Infection | Proportion experiencing post-op infection, determined clinically (treated with antibiotics) | Up to 4 weeks |
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