Pain and Suction Curettage

Not Applicable

Completed

• Conditions: Curettage; Analgesia; Paracervical Block; Paracetamol
• Interventions: Drug: suction curettage; Drug: paracetamol; Other: without drug; Drug: dexketoprofen trometamol

• Registration Number: NCT01947205
• Lead Sponsor: Gökhan Açmaz

Brief 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.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-11
• Primary Completion: 2013-08
• Study Completion: 2013-08
• Status Verified: 2013-09
• Study First Submitted: 2013-09-16
• Study First Submitted QC: 2013-09-19
• Last Update Submitted: 2013-09-19
• Study First Posted: 2013-09-20
• Last Update Posted: 2013-09-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 111

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Arm && Interventions

Group	Intervention	Description
paracervical block with ultracaine	suction curettage	study group
paracetamol	paracetamol	Duration
without drug	without drug	Control group
dexketoprofen trometamol	dexketoprofen trometamol	Study group
two puff xylocain administration on cervical surface	suction curettage	Study group

Primary Outcome Measures

Name	Time	Method
pain reduction	nine months

Trial Locations

Locations (1)

Kayseri Education and Research Hospital of Medicine; 🇹🇷 Kayseri, Turkey