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Dexmedetomidine versus Dexamethasone as an adjuvant to 0.25% Ropivacaine in Ultrasound guided bilateral Rectus Sheath.

Dexmedetomidine versus Dexamethasone as an adjuvant to Ropivacaine in USG- guided Rectus Sheath Block for post-op analgesia in patients undergoing exploratory laparotomy. - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/062115
Enrollment
66
Registered
2024-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Dexmedetomidine versus Dexamethasone as an adjuvant to Ropivacaine in USG- guided Rectus Sheath Block for post-op analgesia in patients undergoing exploratory laparotomy: Group 3 will r

Sponsors

Himalayan Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18-60 years. Physical status ASA I and ASA II Undergoing elective midline abdominal laparotomy under General Anesthesia

Exclusion criteria

Exclusion criteria: Patients aged less than 18 years or more than 60 years Physical status ASA III and ASA IV Allergic to any medication to be used in this study Bleeding diathesis Active skin infection over the area Of injection Patients who shall not give consent.

Design outcomes

Primary

MeasureTime frame
the primary outcome will be measured as the time of first rescue analgesic used which will be the time duration of analgesia produced by the block within 24 hours.Timepoint: the primary outcome will be measured as the time of first rescue analgesic used which will be the time duration of analgesia produced by the block within 24 hours.

Secondary

MeasureTime frame
1.Total opioid consumption over 24 hours. 2. Rates of side effect (nausea, vomiting, pruritis) if any within the first 24 hours. 3.Patient satisfaction utilizing a Likert scale questionnaire on a post-operative day – 4.Adverse drug reaction caused by drugs used if any Timepoint: 0mins, 10mins, 20 mins and 30mins, and then, at 4th hour, 8th hour, 12th hour, 16th hour, 20th hour and 24th hours

Countries

India

Contacts

Public ContactDr Abhimanyu Singh Pokhriyal

himalayan instiute of medical sciences

Pokhriyal.abhimanyu@gmail.com9536997962

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026