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Circumcision, Male clinical trials

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NCT ID: NCT06120634 Completed - Circumcision, Male Clinical Trials

Comparison of Outcomes of Circumcision Via Open and Plastibell Methods

Start date: July 2, 2018
Phase: N/A
Study type: Interventional

Circumcision is considered one of the most common elective surgical procedures, particularly among Muslim and Jewish males. Of all the available techniques, Plastibell is gaining traction amongst surgeons due to its safety in the form of a lower complication rate. The current quasi-experimental study aimed to compare the Open and Plastibell methods of circumcision in a study population which comprised of boys up to 5 years of age who were grouped into the Open method and Plastibell based on parental preference. Follow-up occurred on the 5th, 10th, and, 30th post-procedural day. Basic demographic data, procedural duration, and outcomes were documented.

NCT ID: NCT05764889 Enrolling by invitation - Circumcision, Male Clinical Trials

Study on the Protective Effect of a Flexible Sleeve Penis Protection Device on Penis After Circumcision

Start date: March 15, 2023
Phase: N/A
Study type: Interventional

Circumcision is a common clinical procedure for both circumcision and phimosis, which are common disorders of the male reproductive system. For post-circumcision patients, a flexible sleeve penile protection device was invented as a modification of the traditional gauze bandage. This study investigated the protective effect of the device by recruiting post-circumcision patients to use the device and collecting indicators related to post-operative recovery and patients' experience of using the device.

NCT ID: NCT03761836 Withdrawn - Circumcision, Male Clinical Trials

Evaluation and Adverse Event Surveillance for Initial Implementation of ShangRing Circumcision in Mozambique

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

This is a single-arm interventional study of 1000 male circumcision procedures using the ShangRing device. The primary objective of the study is to enhance understanding of the potential clinical and operational challenges and opportunities that may be associated with widespread use of ShangRing™ device for circumcision in different settings in Mozambique. Specific objectives are: 1) To monitor the proportion of men who choose circumcision through the WHO-prequalified, FDA-approved ShangRing™ device in routine voluntary medical male circumcision (VMMC) service delivery settings where standard surgical methods of circumcisions are available; and 2) To ensure safety during initial implementation of the ShangRing™ device and confirm that adverse event rates are comparable to those found during implementation in other sub-Saharan countries.

NCT ID: NCT03305523 Completed - Circumcision, Male Clinical Trials

The Safety of Thermocautery Usage for Male Children's Circumcisions

MC
Start date: May 1, 2014
Phase: N/A
Study type: Interventional

Since circumcision is a significant workload for surgeons working at the rural state hospitals in Turkey, the use of circumcision techniques that are easy to implement and have low complications is becoming widespread. This research will examine short and long-term complications of male circumcisions using thermocautery technique in light of current literature.

NCT ID: NCT03136224 Completed - Circumcision, Male Clinical Trials

Examination of Short and Long Term Complications of Thermocautery, Plastic Clamping and Surgical Circumcision Techniques

Start date: May 1, 2014
Phase: N/A
Study type: Interventional

Since circumcision is a significant workload for surgeons working at the rural state hospitals in Turkey, the use of circumcision techniques that are easy to implement and have low complications is becoming widespread. In this study, thermocautery, plastic clamping, and conventional (open surgical) circumcision techniques were compared to each other in terms of their short and long term complications.

NCT ID: NCT02593630 Completed - Circumcision, Male Clinical Trials

Unicirc Adolescent 12-15 Year Old Boys

Start date: April 2016
Phase: Phase 4
Study type: Interventional

This is a field case series of Unicirc under topical anaesthetic among adolescent boys, aged 12 to 15 years.

NCT ID: NCT02587208 Recruiting - Circumcision, Male Clinical Trials

Plastibell Versus Conventional Dissection Techniques for Circumcision in Infants and Children

Start date: January 2015
Phase: N/A
Study type: Interventional

Outcome of circumcision with Plastibell or conventional dissection techniques in infants and children: A prospective randomized controlled trial Aim: to evaluate and compare postoperative and esthetic outcomes after Plastibell and conventional dissection circumcision Methods: Randomized Controlled Trial Inclusion criteria: patients younger than 13 years including neonates who required circumcision for various indications. Exclusion criteria: - patients with bleeding or clotting disorders - Those whose parents insisted on a particular type of surgery - Children with lateral- lateral diameter of the glans over which a Plastibell device could not be placed Primary endpoint: parental concerns and satisfaction (questionnaire) Secondary endpoints: composite morbidity, operative time, postoperative pain (analgesic requirements) - Early postoperative problems: infection, bleeding, swelling, dysuria, pain (incidence, mean duration, emergency care if necessary, parental concerns about them (on a Likert-type 5-point scale [ not at all, a little, rather, very, very much]) - Irregular scar, jumbling of tissues at the site of frenulum (assessed by physician) - Postoperative adhesions (assessed by physician) - Postoperative pain and analgesic requirements (paracetamol 15 mg/kg PO Q6 hrs for 48 hrs then PRN) number of doses and days required for analgesia as judged by parents, VAS ( >- 6 SCORE ), Kaplan-Meier analysis (time to event) - Parental satisfaction ( overall esthetic outcome [ very much satisfied, very satisfied, rather, a little satisfied, not at all satisfied]) - Parental satisfaction ( skin removal): excess skin removal, insufficient skin removal [ not at all, a little, rather, very, very much] - Time for bell separation (mean +-SD), Kaplan-Meier analysis for different age groups

NCT ID: NCT02511548 Not yet recruiting - Circumcision, Male Clinical Trials

Increasing Medical Male Circumcision Uptake

Start date: August 2015
Phase: Phase 3
Study type: Interventional

The main objective of this study is to reach 80% circumcised men in a random sample of men living in the township of Orange Farm (South Africa).

NCT ID: NCT02443792 Completed - Circumcision, Male Clinical Trials

Unicirc vs Open Surgical Circumcision

Unicirc004
Start date: April 2015
Phase: Phase 4
Study type: Interventional

RCT of Unicirc under topical anesthetic w/ cyanoacrylate wound sealing vs. open surgical circumcision under local anesthetic with suturing.

NCT ID: NCT02337179 Completed - HIV Clinical Trials

Male Circumcision Services for HIV Prevention in the Dominican Republic

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the feasibility of introducing voluntary medical male circumcision as a form of HIV prevention in high HIV prevalence areas in the Dominican Republic.