Paracetamol Rectal Suppository for postoperative pain reduction in Abdominal Hysterectomy A Randomized controlled trial

Not Applicable

Completed

• Conditions: healthy woman and no underlying disease; Renal and Urogenital - Other renal and urogenital disorders; Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

• Registration Number: ACTRN12612000531819
• Lead Sponsor: Khon Kaen Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-05-21
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Elective benign abdominal hysterectomy
Age <70 years
Body weight 30-80 kg

Exclusion Criteria

paracetamol hypersensitivity
Bleeding disorders
Had underlying diseases
Renal, hepatic dysfunction

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
postoperative pain in abdominal hysterectomy using questionnaires and visual analog scale (VAS)[at 6 months after randomization]

Secondary Outcome Measures

Name	Time	Method
Adverse effects such as nausea vomiting, fever using questionnaire[at 6 months after randomization];Opioids consumption using medical records[at 6 months after randomization]