Comparison of postoperative urinary retention and pain control between intrathecal nalbuphine and intrathecal morphine in anorectal surgery

Phase 4

Completed

• Conditions: rinary retentionPain scoreNausea & vomitting scorePruritus scoreSedation score; Urinary retention; Nalbuphine; Morphine; Bupivacaine; Anorectal surgery; Spinal anesthesia

• Registration Number: TCTR20240328010
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2023-08-04
• Study Start: 2024-03-28
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

1. Age 18-65 years old
2. ASA physical status I-III
3. Undergoing elective anorectal surgery with spinal anesthesia at Chulalongkorn Hospital

Exclusion Criteria

1. Allergies to drugs used in the study
2. Inability to provide pain scores
3. History of prior urinary catheterization
4. Chronic pain persisting beyond 3 months and prior exposure to morphine
5. Presence of skin diseases and itching
6. The requirement for critical care post-surgery
7. Contraindications to the specific spinal anesthesia employed in the study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Incidence of urinary retention 24 hour percentage

Secondary Outcome Measures

Name	Time	Method
Pain score (movement & rest) 24 hour numeric rating scale,Nausea & vomiting 24 hour Nausea & Vomiting score,Pruritus 24 hour Verbal rating scale,Sedation 24 hour Ramsay sedation scale