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Ultrasound guided Scalp Block for brain surgery- A randomized trial

Ultrasound guided Scalp Block versus anatomical landmark guided scalp block in neurosurgical patients- A prospective randomized trial - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/068003
Enrollment
96
Registered
2024-05-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: S06- Intracranial injury Health Condition 2: C71- Malignant neoplasm of brain Health Condition 3: C700- Malignant neoplasm of cerebral meninges Health Condition 4: C715- Malignant neoplasm of cerebral ventricle Health Condition 5: S066- Traumatic subarachnoid hemorrhage Health Condition 6: S065- Traumatic subdural hemorrhage

Interventions

Intervention1: Ultrasound guided scalp block: Frequency 1 Duration 12 minutes (approximately) for application Control Intervention1: Anatomical landmark guided scalp block: Frequency 1 Duration 8 min

Sponsors

Indira Gandhi Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age 18 years and above undergoing neurosurgery

Exclusion criteria

Exclusion criteria: (i) Refusal to participate in the study (ii) Fracture or hematoma over the site of application of scalp block (iii) Contra-indication to the anesthetic drugs being used in this study protocol (iv) ASA IV,V and VI patient (v) Patients who underwent endotracheal intubation outside the operation theater.

Design outcomes

Primary

MeasureTime frame
The comparison of level and duration of analgesia in patients receiving ultrasound guided scalp block versus anatomical landmark guided scalp blockTimepoint: (i)- at time of shifting out from PACU (ii)- 3 hours after end of anesthesia procedure (iii)- 6 hours after end of anesthesia procedure

Secondary

MeasureTime frame
(i) Comparison of, time of demand of first analgesic drug postoperatively between the two groups. (ii) To compare Critical care pain observation tool (CPOT) post-operatively between the two groups.Timepoint: (i)- at time of shifting out from PACU (ii)- 3 hours after end of anesthesia procedure (iii)- 6 hours after end of anesthesia procedure

Countries

India

Contacts

Public ContactKunal Kumar

Indira Gandhi Medical College, Shimla

kunaal_kumar@yahoo.com9945602747

Outcome results

None listed

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