Skip to content

To study the effect of drug in patients undergoing upper limb surgeries via nerve block

Effect of buprenorphine as an adjunct to local aneasthetic mixtures in ultrasound guided supraclavicular brachial plexus block in patients undergoing upper limb surgeries - a Randomized Controlled study. - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066998
Enrollment
56
Registered
2024-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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: buprenorphine: patients will be given 300mcg of buprenorphine along with 9ml of 0.5% bupivacaine + 9ml of 2% lignocaine with adrenaline in ultrasound guided supraclavicular brachial ple

Sponsors

Pondicherry Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.patients undergoing elective elbow,forearm ,hand surgeries. 2.aged between 18 and 60 years of either gender 3.patients belonging to ASA physical status 1, 2

Exclusion criteria

Exclusion criteria: 1.BMI more than or equal to 35kg per meter squared. 2.allergy to local anesthetics/opioids 3.patients on opioids for chronic use 4.puncture site infection 5.preexisting nerve injury 6.coagulopathy.

Design outcomes

Primary

MeasureTime frame
duration of sensory blockade in ultrasound guided supraclavicular brachial plexus block in patients undergoing upper limb surgeries.Timepoint: duration of sensory blockade is assessed from the time of onset of sensory blockade to complete resolution of blockade. it will be assessed every hour in the first 16 hours in the postoperative period .

Secondary

MeasureTime frame
1.time taken for onset of sensory and motor blockade 2.duration of motor blockade 3.level of sedation using ramsay sedation scale 4. to assess hemodynamic effectsTimepoint: the above mentioned parameters are assessed intraoperatively and postoperatively every hour for the first 16 hours

Countries

India

Contacts

Public ContactDr. Thenmozhi

Pondicherry Institute of Medical Sciences

ajstyle.bt@gmail.com9791853400

Outcome results

None listed

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