To Compare Efficacy of dexmedetomidine as an adjuvant to levobupivacaine in infraumbilical surgeries under spinal anaesthesia

A randomised controlled study on efficacy of dexmedetomidine as an adjuvant to levobupivacaine in infraumbilical surgeries under spinal anaesthesia, at SMS Medical College and attached group of hospital, Jaipur - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/071424

Enrollment

Registered

2024-07-26

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Normal saline : Patients will be receiving Isobaric Levobupivacaine 0.5 percent 15mg with 0.3ml normal saline total volume made 3.3ml. Control Intervention1: dexmedetomidine : Patien

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing infraumbilical surgeries under spinal anaesthesia 2. Patients giving consent for the participation. 3. Patients belonging to American society of anaesthesiologist ASA Class I and II.

Exclusion criteria

Exclusion criteria: 1. Patient should not be a part of other study 2. Non cooperative patient 3. Patient refused to undergo procedure 4. Patient who were pregnant or lactating 5. Patient who having some coagulating or neurological disorder 6. Patient with spine injury or previous spine surgery ,sepsis over spine 7. Patient with morbid obesity 8. Patients having allergy to study drugs 9. Any life threatening disease

Design outcomes

Primary

Measure	Time frame
1. Mean Time taken for onset of Sensory block min 2. Mean duration of Sensory block (min) 3. Mean Time taken for onset of Motor block min 4. Mean duration of Motor block min 5. Proportion of cases with different maximum level of sensory block achieved. 6. Mean time taken to achieve maximum level of sensory blockTimepoint: 90 min	—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Rohit Dusad

Sms MedicalCollege And Attached Hospital

rajnimathur@hotmail.com9829357194

Outcome results

None listed

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