Viewing Study NCT00188071



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00188071
Status: COMPLETED
Last Update Posted: 2017-11-01
First Post: 2005-09-12

Brief Title: Postoperative Pain After Medical Abortion Under Local Anesthesia Comparison of Several Analgesic Regimen
Sponsor: University Hospital Angers
Organization: University Hospital Angers

Study Overview

Official Title: Postoperative Pain After Medical Abortion Under Local Anesthesia a Prospective and Randomized Trial Comparing Several Analgesic Regimen
Status: COMPLETED
Status Verified Date: 2005-09
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: To compare postoperative analgesia by paracetamol 1gr or ketoprofen 100 mg or the combination of these two analgesics
each treatment beeing allocated by randomization
Detailed Description: 240 pregnant women who undewent a medical abortion by aspiration under local anesthesia day case surgery were enrolled after informed consent and signed approval
according to randomization they received one hour before medical abortion procedure performed under local anesthesia of the cervix one of these three diffrente analgesics

paracetamol 1 gr
ketoprofen 100 mg
the association of both Postprocedure pain was recorded by nurse using a visual analog scale VAS 7 times before and after the procedure until the discharge of the patient
if VAS was above 40 on two consecutive measurements a morphine injection was given
the number and total amount of morphine was recorded
satisfaction was recorded within the 3 postoperative day by a telephone inquiry

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