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Effect of scalp block with dexmedetomidine and ropivacaine on pain

Effect of scalp nerve block with dexmedetomidine as an adjuvant to ropivacaine on postoperative pain in patients undergoing supratentorial craniotomy: A double-blind randomized study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104134
Enrollment
36
Registered
2026-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: D496- Neoplasm of unspecified behavior of brain Health Condition 2: G978- Other intraoperative and postprocedural complications and disorders of nervous system

Interventions

Intervention1: Scalp block with adjuvant: Scalp block will be given with one microgram per kg dexmedetomidine diluted to one ml and mixed with 20 ml of 0.5 percent ropivacaine. Duration of interventio

Sponsors

All India Institute of Medical Sciences New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA physical status: I to III. 2.Scheduled for elective supratentorial craniotomy under general anaesthesia. 3.GCS (Glasgow Coma Scale) score of 15 before surgery. 4.Planning to extubate at the end of surgery.

Exclusion criteria

Exclusion criteria: 1.Patient refuses treatment 2.Known allergy or hypersensitivity to local anesthetics such as ropivacaine or to dexmedetomidine 3.Coagulopathy or being on anticoagulant therapy 4.Infection at the scalp block injection site 5.Pre-existing neurological deficits or cognitive impairments 6.Chronic pain syndrome or regular use of analgesics (more than 1 week) or opioids 7.Severe cardiovascular, liver, or kidney disease 8.Patients who are not expected to be extubated immediately after the surgical procedure

Design outcomes

Primary

MeasureTime frame
Duration of adequate analgesia or Pain-free intervalTimepoint: Time in minutes from the completion of the scalp block to the patients first request for rescue analgesia that is NRS more than 4

Secondary

MeasureTime frame
Pain Intensity Rescue Analgesic Consumption Hemodynamic stability Sedation Level Patient Satisfaction Adverse Events Timepoint: arrival in NICU, 2, 4, 8, 12, and 24 hours after surgery

Countries

India

Contacts

Public ContactMedha Gupta

All India Institute of Medical Sciences, New Delhi

medhagupta6269@yahoo.com9990814780

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026