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NCT01947205 Clinical Trial

Pain and Suction Curettage

Analgesia Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01947205
Other study ID # Kayseri ERH
Secondary ID KayseriERH
Status Completed
Phase N/A
First received September 16, 2013
Last updated September 19, 2013
Start date November 2012
Est. completion date August 2013

Study information
Verified date September 2013
Source Kayseri Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 111
Est. completion date August 2013
Est. primary completion date August 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 16 Years to 45 Years
Eligibility 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

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• paracetamol

• dexketoprofen trometamol

• suction curettage

• suction curettage

Other:
• without drug

Locations
Country Name City State
Turkey Kayseri Education and Research Hospital of Medicine Kayseri

Sponsors (1)
Lead Sponsor Collaborator
Gökhan Açmaz

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain reduction nine months Yes
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