IRCT20190417043295N1
Completed
Phase 4
Comparison of sedative effect of dexmedetomidine and midazolam in patients undergoing EUS procedure outside the operating room
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Condition 1: patients undergoing gastrointestinal Endosonography outside the operating room. Condition 2: .
- Sponsor
- Ahvaz University of Medical Sciences
- Enrollment
- 126
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Candidates for gastrointestinal endosonography
- •Declaration of consent for entry into the study and signature of the consent form
- •Anesthesia ASA class I and II
- •Age range 18 to 65 years
Exclusion Criteria
- •Renal Failure
- •Liver Failure
- •Sensitivity to the drugs studied
- •Drug addiction
- •Chronic pain syndromes
- •Cardiovascular disease
- •Respiratory disease
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not yet recruiting
Phase 4
A study conducted in a tertiary care hospital comparing the sedative effects of Dexmedetomidine and Propofol infusion during middle ear operations.CTRI/2023/07/055887Dr. Chandamita Bhagabati
Not yet recruiting
Not Applicable
Comparison between sedation efficacy of drugs(dexmedetomidine and ketamine)versus (propofol and ketamine) for(ICRT) applicator insertion in cervical cancer patientsCTRI/2022/11/047737CMCH BHOPA
Not yet recruiting
Phase 4
Comparison of sedation efficacy of the two sedative agents: Dexmedetomidine and Midazolam in critically ill childreCTRI/2024/06/068582AIIMS Raipur
Completed
Phase 2
A comparison of sedative effect with dexmedetomidine -fentanyl versus midazolaml–fentanyl during cataract surgery with phacoemulsification techniqueCataract surgery.Cataract in diseases classified elsewhereIRCT20180416039326N3Esfahan University of Medical Sciences70
Completed
Not Applicable
Examination of sedative effects of dexmedetomidine during chronic subdural hematoma surgery under local anesthesia: prospective randomized control trialChronic subdural hematoma patientJPRN-UMIN000013904ihon University School of Medicine40