Sedation using Ketofol versus Fentanyl + Propofol in patients undergoing Lower Gastrointestinal Endoscopy: a randomized trial

Phase 2

Terminated

• Conditions: Analgesia; Colonoscopy

• Registration Number: RBR-4mvny8s
• Lead Sponsor: Hospital São Domingos

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-07-28
• Study Start: 2023-08-26
• Last Update Posted: 18 September 2023

Recruitment & Eligibility

• Status: Terminated
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

After approval by the Research Ethics Committee of the Hospital and the Free and Informed Consent Term (APPENDIX C) signed, patients aged 18 to 65 years, ASA I-II, undergoing elective colonoscopy in a private hospital in São Luís - MA.

Exclusion Criteria

Patients who refuse to participate or who have: pregnancy, active gastrointestinal bleeding, ASA III-V, history of hypersensitivity to the drugs used in this research, epilepsy, severe heart failure, severe respiratory failure, increased intracranial pressure and /or hemodynamic instability such as peripheral oxygen saturation = 90%, systolic blood pressure (SBP) < 60 mmHg and heart rate = 40 bpm.

Study & Design

• Study Type: Intervention
• Study Design: Not specified