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Dexamethasone Dose Comparison as an Adjuvant to Levobupivacaine in Lower Abdominal Surgery.

Comparison of Two Different Doses of Dexamethasone as an Adjuvant to Intrathecal Levobupivacaine on Analgesic Efficacy in Lower Abdominal Surgeries: A Randomised Controlled Study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091982
Enrollment
50
Registered
2025-07-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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: Subarachnoid block: Subarachnoid block with 0.5% isobaric levobupivacaine with 2mg of dexamethasone as an adjuvant will be given to patients undergoing lower abdominal surgeries, 15 min

Sponsors

UCMS and GTB Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to ASA grade I or II, between 18-65 years of age, and height 150-180 cm, scheduled for lower abdominal surgeries under subarachnoid block will be included in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria Non-consenting for subarachnoid block Infection at injection site Coagulopathy Drugs addicts and chronic alcoholics Any spine deformity On antiarrhythmics Patients with history suggestive of space occupying lesion, increased intracranial tension, seizure disorder, pre-existing neurological deficit, hepatic and renal disease and pre-existing diabetes mellitus.

Design outcomes

Primary

MeasureTime frame
Duration of effective analgesia with two different doses of dexamethasone as an adjuvant to nitrate al levobupivacaine in lower abdominal surgeriesTimepoint: The time from the subarachnoid block to the time of patient s first complaint of pain VAS more than equal to 3 and till 24 hours from subarachnoid block

Secondary

MeasureTime frame
Quality of sensory block Quality of motor block Side effects nausea, vomitting, hypotension, bradycardia, hyperglycaemia, hypernatremia & othersTimepoint: The time from the subarachnoid block to the time of first complaint of pain VAS more than equal to 3 & till 24 hours from subarachnoid block

Countries

India

Contacts

Public ContactDr TENZIN SONAM

University College of Medical Sciences and GTB Hospital

rsramb@gmail.com9871741419

Outcome results

None listed

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