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EFFECT ON SENSORY BLOCK DURATION IN INGUINAL HERNIA PATIENTS OF 18 - 60 YEARS AFTER SPINAL ANAESTHESIA WITH BUPIVACAINE SUPPLEMENTED WITH DEXAMETHASONE

Effect on sensory block duration after spinal anesthesia supplemented with intravenous Dexamethasone. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075564
Enrollment
60
Registered
2024-10-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: K40-K46- Hernia Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Dexamethasone: Spinal Anesthesia with 3 ml of 0.5% bupivacaine(heavy) with 8 mg of dexamethasone(2ml) given intravenously Control Intervention1: Normal saline: Spinal anaesthesia with 3

Sponsors

Dibyanshu Shekhar Swain
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists (ASA) physical status I and II patients in the age group of 18–60 years posted for elective unilateral open inguinal hernia surgeries.

Exclusion criteria

Exclusion criteria: Patients with a history of allergy to drugs used in the study, a history of substance abuse, with a body mass index (BMI) =35 and patients with psychosis/gross neurological disorders will be excluded.

Design outcomes

Primary

MeasureTime frame
Sensory block durationTimepoint: Intra-operative period

Secondary

MeasureTime frame
1) To determine the time taken to achieve highest level of sensory block. 2) To determine Time required to first rescue analgesia. 3) To determine the Effects on hemodynamics of the patient. 4) To find incidence of postop nausea & vomiting.Timepoint: At baseline, every 5 min for up to 30 min & then every 15 min until two-dermatome regression from the highest dermatome blocked.

Countries

India

Contacts

Public ContactDibyanshu Shekhar Swain

AIIMS Raipur

drpradeepk1117@gmail.com9820961117

Outcome results

None listed

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