Overview
Pain and Suction Curettage
Status:
Completed
Completed
Trial end date:
2013-08-01
2013-08-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
Aim of the study was to investigate the analgesic efficacy of preoperative oral dexketoprofen trometamol, intravenous paracetamol, lidocaine spray and paracervical block with ultracaine on curettage procedure.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Gökhan AçmazTreatments:
Acetaminophen
Carticaine
Dexketoprofen trometamol
Ketoprofen
Criteria
Inclusion Criteria:- pregnant participants between 35-48 days of gestation (5 to 7 weeks of gestation)
pregnant participants with a single viable intrauterine pregnancy requesting
termination of pregnancy.
Exclusion Criteria:
incomplete abortions, diabetes mellitus, tendency to bleed such as thrombocytopenia, factor
deficiency and functional disorders of platelets… etc, pelvic infection, known cervical
stenosis, significantly impaired respiratory or cardiac conduction functions, active liver
disease, renal disease, previous adverse reaction to any of the drugs used in the study,
and patients who are unable to understand how to score a 10-cm visual analog scale (VAS)
pain score. Moreover, patients who described chronic pelvic pain prior to the study or
patients who rated their pain level on a continuous 100-mm VAS different from 0 (no pain)
just before the study were not included into study.