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A comparison of morphine and dexmedetomidine in spinal anesthesia for patients undergoing infraumbilical surgeries

Comparative evaluation of intrathecal morphine versus dexmedetomidine in patients undergoing infraumbilical surgeries under spinal anesthesia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094583
Enrollment
70
Registered
2025-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: N813- Complete uterovaginal prolapse

Interventions

Intervention1: Dexmedetomidine: 5mcg,intrathecal,18 months Control Intervention1: Morphine: 0.25mg,Intrathecal,18months

Sponsors

Keerthana N D
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient willing to provide informed written consent 2)ASA physical status grade land ll 3)Patient scheduled to undergo elective infraumbilical surgeries under spinal anesthesia

Exclusion criteria

Exclusion criteria: 1)Patient allergic to local anesthesia 2)Patient having any Absolute contraindication for spinal anesthesia 3)Acute or chronic respiratory disease 4)Cognitive or psychiatric disturbances 5)Hypertension or other cardiovascular abnormalities 6)Patient with heart block 7)Patient on beta blockers

Design outcomes

Primary

MeasureTime frame
To compare analgesic efficacy in terms of duration of analgesia of adjuvant dexmedetomidine and morphine in spinal anesthesiaTimepoint: 18months—

Secondary

MeasureTime frame
To compare characteristics of spinal blockTimepoint: 18months;To compare perioperative hemodynamic parametersTimepoint: 18months;To compare any adverse effects if anyTimepoint: 18months—

Countries

India

Contacts

Public ContactDr Keerthana N D

Bangalore medical college and research institute

drmadhumala@gmail.com9886786768

Outcome results

None listed

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