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comparison of stellate ganglion block with interscalene brachial plexus block for post operative pain relief in patients undergoing surgeries of upper limb

Stellate Ganglion Block vs Interscalene Brachial Plexus Block for postoperative analgesia among patients undergoing upper limb surgeries: randomized clinical trial. - NL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067005
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: S423- Fracture of shaft of humerus

Interventions

Intervention1: stellate ganglion block: patients with upper limb fractures will be administered stellate ganglion block for post operative analgesia. patients will be observed for post operative pain

Sponsors

PGIMER chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA physical status 1–2, aged between 18 and 60 years with an upper limb fracture scheduled for surgery under general anaesthesia. We will include patients with humerus shaft fractures, humerus surgical neck fractures and humeral supracondylar fractures, where open surgery is indicated.

Exclusion criteria

Exclusion criteria: BMI more than 30 kg/m2, history of substance abuse, Inability to understand a pain scale (VAS, NRS), Allergy to lignocaine , Chronic sympathetic-mediated pain syndromes affecting the upper limb, Trauma other than to the affected limb, Severe congestive heart failure , Severe Chronic obstructive pulmonary disease (COPD)

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of preoperative stellate ganglion block with interscalene brachial plexus block among patients undergoing upper limb surgeries as a difference in NRS of 2.Timepoint: 0,6,12,24 hours

Secondary

MeasureTime frame
To determine the incidence of adverse effects in each of the two groups, To determine time to administration of first rescue analgesic, To find the total dose of tramadol consumption in first 48 hours post operatively Timepoint: 0,6,12,24 hours

Countries

India

Contacts

Public ContactDr Karan Singla

PGIMER Chandigarh

karansingla16@gmail.com9592919073

Outcome results

None listed

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