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Phimosis clinical trials

View clinical trials related to Phimosis.

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NCT ID: NCT04902898 Recruiting - Phimosis Clinical Trials

Safety and Efficacy of the Sterile Single-use Circular Stapling Device CIRCCURER II (Jiangxi Langhe Medical Instrument Co., Ltd., Guangzhou, China)

CiCi-2021
Start date: May 11, 2021
Phase: N/A
Study type: Interventional

Evaluation of the safety and efficacy of the sterile single-use circular stapling device CIRCCURER II (Jiangxi Langhe Medical Instrument Co., Ltd., Guangzhou, China) in comparison with circumcision in adults patients with pathological foreskin (phimosis, stenosis, redundant prepuce)

NCT ID: NCT04646967 Recruiting - Pain, Postoperative Clinical Trials

An Evaluation of Pain Outcomes of Ketorolac Administration in Children Undergoing Circumcision

Start date: November 25, 2022
Phase: Phase 2
Study type: Interventional

Circumcision is the most common surgical procedure performed by Pediatric Urologists. Ketorolac has been shown to have an efficacy similar to morphine in multi-modal analgesic regimens without the commonly associated adverse effects. This study aims to see if giving ketorolac during the operation will result in better pain control. We hypothesize that ketorolac will result in pain control similar to morphine with a lower incidence of side effects such as nausea and vomiting.

NCT ID: NCT03931850 Recruiting - Phimosis Clinical Trials

Does Neurostimulation Improve Efficacy for Ultrasound-Guided Transperineal Pudendal Nerve Block In Children

Start date: April 30, 2019
Phase: N/A
Study type: Interventional

This study aim to compare efficacy of transperineal pudendal nerve block between 2 techniques, by dual guidance (ultrasound and neurostimulation) vs by ultrasound-guided only, in pediatric patients who undergo circumcision. Primary outcome : Block efficacy will be assessed from ratio of patients who receive opioids in immediate postoperative period. Secondary outcomes : - This study also measure other aspects of pain which can reflect the block efficacy including pain score in 24 hours, postoperative analgesic requirement in 24 hours, time to first analgesia, block success rate. - Block performance : imaging time, needling time, total performance time, - Block safety : collect complications from block including vascular/rectal puncture, bleeding (hematoma), local anesthetic systemic toxicity, voiding difficulty - Parental satisfaction will be also collected which scoring use 1-5 metric.

NCT ID: NCT01108198 Recruiting - Phimosis Clinical Trials

Treatment of Phimosis With Topical Steroid Cream -Double-blind, Randomized, Placebo-controlled Study

Start date: October 2006
Phase: Phase 4
Study type: Interventional

During last years topical steroid creams have been suggested to be effective treatment for non-retractable foreskin instead of circumcision. Aim of this study is to investigate the efficacy, safety and persistence of treatment results of a medium potent steroid cream in a double-blind, randomized, placebo-controlled study.