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Office Hysteroscopy clinical trials

View clinical trials related to Office Hysteroscopy.

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NCT ID: NCT05610371 Completed - Anesthesia, Local Clinical Trials

Intrauterine Anesthesia in Operative, Awake, Office Hysteroscopy. A Randomized Double-blind Placebo-controlled Trial

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

Objective: to evaluate intrauterine lidocaine infusion effectiveness in reducing pain associated with operative, awake office hysteroscopy Methods: A total of 100 patients will be randomized for this study The control group underwent hysteroscopy using a saline distension medium. The study group underwent hysteroscopy using 10ml of 2% lidocaine that was added to the first liter of distension medium. Patients quantified their pain using a 0-10 VAS score, at the following five predefined points: baseline, before the procedure; while inserting the hysteroscope through the cervix; during the operative procedure; immediately after the procedure and 15 minutes following the procedure.

NCT ID: NCT05246436 Completed - Office Hysteroscopy Clinical Trials

Effect of Warm Fluid Distension Media in Relieving Pain in Outpatient Hysteroscopy

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The aim of study is to determine if the use of warm saline distention media during outpatient hysteroscopy reduces Pain/discomfort of the procedure. Research hypothesis: In women undergoing office hysteroscopy, there will be reduced pain perception when using warm saline (body temperature 37°C during office hysteroscopy. Research question: In women undergoing office hysteroscopy, Will there be a difference in pain perceived during the procedure if the investigators use warm saline(body temperature 37°C) rather than normal saline (room temperature) as a distension media?

NCT ID: NCT04044079 Completed - Office Hysteroscopy Clinical Trials

Vaginal Dinoprostone Versus Vaginal Misoprostol Prior to Diagnostic Office Hysteroscopy in Postmenopausal Patients

Start date: August 20, 2019
Phase: Phase 4
Study type: Interventional

To compare the effectiveness of vaginal dinoprostone and vaginal misoprostol with placebo in minimizing the pain experienced by postmenopausal patients during diagnostic office hysteroscopy and to assess the ease of insertion of hysteroscope as reported by the hysteroscopist.

NCT ID: NCT03683914 Completed - Office Hysteroscopy Clinical Trials

Vaginal Dinoprostone Prior to Diagnostic Office Hysteroscopy in Postmenopausal Patients

Start date: September 30, 2018
Phase: Phase 4
Study type: Interventional

To compare the effectiveness of vaginal dinoprostone with placebo in minimising the pain experienced by postmenopausal patients during diagnostic office hysteroscopy and to assess the ease of insertion of hysteroscope as reported by the hysteroscopist.