Skip to content

Comparative study between intravenous Magnesium Sulphate and intravenous Dexmedetomidine for pain relief after lower abdominal surgeries under spinal anesthesia

An observational study to compare the post operative analgesic effect of intravenous magnesium sulphate versus intravenous dexmedetomidine in infra umbilical surgeries under subarachnoid block. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/11/097009
Enrollment
220
Registered
2025-11-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Control Intervention1: Nil as an observational study: Nil as an observational study

Sponsors

R G Kar Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who understand procedure and can give written consent. Patients who understand VAS score. Patients who are hemodynamically stable.

Exclusion criteria

Exclusion criteria: Pregnant and lactating mother. Patients with history of magnesium sulphate or dexmedetomidine allergy. Patients with history of drug and alcohol consumption. Patients on treatment with CCB. Patients who have liver disease. Patients who have cardiac disease. Haematological disorders or musculoskeletal disorders. Patients having renal disease. Neurological deficit or psychological disorder. Uncontrollable diabetes. Immunocompromised patients. Failed spinal converted to general anaesthesia.

Design outcomes

Primary

MeasureTime frame
Postoperative analgesia measured by VAS Time to rescue analgesia and number of doses requiredTimepoint: 0, 6, 12, 24 hours

Secondary

MeasureTime frame
To compare the onset and maximum level of sensory block. To compare onset and duration of motor block. To observe hemodynamic parameters like hypotension,bradycardia and respiratory depression.Timepoint: 0,6,12,24 hours

Countries

India

Contacts

Public ContactDr Bani Parvati Magda Hembrom

R G Kar Medical College and Hospital

banihembrom72@gmail.com9903207690

Outcome results

None listed

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