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Evaluation of addition of Intrathecal Dexmedetomidine to 1% 2-Chloroprocaine in spinal anaesthesia for short duration surgeries.

Evaluation of addition of Intrathecal Dexmedetomidine to 1% 2-Chloroprocaine in spinal anaesthesia for short duration surgeries: A Prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/033128
Enrollment
60
Registered
2021-04-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: S970- Crushing injury of ankle Health Condition 2: N430- Encysted hydrocele Health Condition 3: N471- Phimosis Health Condition 4: S881- Traumatic amputation at level between knee and ankle Health Condition 5: S980- Traumatic amputation of foot at ankle level

Interventions

Intervention1: Addition of intrathecal Dexmedetomidine to 1% 2-chloroprocaine in spinal anaesthesia: Evaluation of addition of Dexmedetomidine to 1% 2-chloroprocaine in spinal anaesthesia for short du

Sponsors

Dr Abhishek Zala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grading 1,2. Patient posted for lower limb short duration surgeries. Patient able to give verbal and informed consent. Patient able to understand VAS regarding assessment of pain.

Exclusion criteria

Exclusion criteria: Patient not willing. Allergy to local anaesthetic. Contraindication of spinal, regional anaesthesia. Patient with coagulopathy, local infection. Patient with preexisting neurological deficits. Patient with history of drug or alcohol abuse, psychiatric illness. Patient with pelvic fracture.

Design outcomes

Primary

MeasureTime frame
Duration of Analgesia and requirement of first analgesic dose after surgeryTimepoint: Duration of Analgesia and requirement of first analgesic dose after surgery

Secondary

MeasureTime frame
Vital parameter and complication associated with blockTimepoint: Vital parameters will be monitored before giving spinal anesthesia, immediately after giving spinal anesthesia at 2,5,10,30,60 minutes

Countries

India

Contacts

Public ContactDr Komal Modi

Government Medical College and SSG Hospital, Vadodara

komaltmodi@gmail.com

Outcome results

None listed

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