Viewing Study NCT02943135


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Ignite Modification Date: 2026-02-20 @ 12:37 PM
Study NCT ID: NCT02943135
Status: COMPLETED
Last Update Posted: 2020-05-20
First Post: 2016-10-21
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Lidocaine In-situ Gel Before Intrauterine Device Insertion
Sponsor: Assiut University
Organization:

Study Overview

Official Title: Effect of Self-administered Lidocaine In-situ Gel on Intrauterine Device Insertion Pain: A Randomized Controlled Trial
Status: COMPLETED
Status Verified Date: 2020-05
Last Known Status: None
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: Intrauterine device can cause pain and discomfort in several ways: Use of the tenaculum to grasp the cervix and straighten the uterus for proper insertion; trans-cervical actions including measuring uterine depth, inserting the insertion tube, and removing the tube; and placement of the device in the uterus.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: