Viewing Study NCT04500496



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Last Modification Date: 2024-10-26 @ 1:41 PM
Study NCT ID: NCT04500496
Status: UNKNOWN
Last Update Posted: 2021-09-29
First Post: 2020-08-03

Brief Title: Vaginal Dinoprostone Versus Isonicotinic Acid Hydrazide Prior to Diagnostic Office Hysteroscopy
Sponsor: Aswan University Hospital
Organization: Aswan University Hospital

Study Overview

Official Title: Vaginal Dinoprostone Versus Vaginal Isonicotinic Acid Hydrazide Prior to Diagnostic Office Hysteroscopy in Postmenopausal Patients a Randomized Controlled Trial
Status: UNKNOWN
Status Verified Date: 2021-09
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To compare the effectiveness of vaginal dinoprostone and vaginal Isonicotinic acid hydrazide 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
Detailed Description: hysteroscopy is commonly used in the diagnosis and treatment of intrauterine lesions such as polyps fibroids septa and adhesions and in the presence of abnormal bleeding and during the removal of an intrauterine device or foreign body Cervical ripening is made possible by the use of medication through different routes

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None