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Clinical Trials/NCT05679765
NCT05679765
Completed
Phase 4

Analgesic Efficacy of Ultrasound-guided Greater Occipital Nerve Block in Patients of Chronic Migraine

Pain Medicine Department1 site in 1 country50 target enrollmentApril 1, 2022

Overview

Phase
Phase 4
Intervention
Greater Occipital Nerve Block with dexamethasone and lidocaine
Conditions
Chronic Migraine
Sponsor
Pain Medicine Department
Enrollment
50
Locations
1
Primary Endpoint
Analgesic efficacy
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The study was carried to determine the analgesic efficacy of greater occipital nerve block in patients of migraine. It was a randomised controlled which took place from april 2022 - october 2022. Fifty patients suffering from migraine were included in the study. Patients in Group G were given greater occipital nerve block (GONB) with lignocaine and dexamethasone under ultrasound guidance while those in Group S were given saline 0.9% as placebo. Pain score using Numeric Rating Scale and number of headache days was assessed at four,eight and twelve weeks after the procedure as a primary outcome. Total headache days were recorded as a secondary outcome.

Registry
clinicaltrials.gov
Start Date
April 1, 2022
End Date
August 31, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Pain Medicine Department
Responsible Party
Principal Investigator
Principal Investigator

Moazzam Ali

Doctor, Head Of Department

Pain Medicine Department

Eligibility Criteria

Inclusion Criteria

  • Patients between 18 to 60 years
  • diagnosed case of migraine

Exclusion Criteria

  • Patients with known allergies to local anaesthetics
  • pregnancy
  • history of cranial or cervical surgery
  • head injury
  • headaches secondary to medication overuse
  • patients with uncontrolled systemic disease like blood pressure, diabetes mellitus
  • hypo or hyperthyroidism
  • patient who had already received GONB or botulinum toxin type A therapy within last 6 months
  • major psychiatric disorder
  • history of chronic pain syndromes

Arms & Interventions

Group G

Greater occipital nerve block (GONB) under ultrasound guidance with lidocaine and dexamethasone on the side of headache

Intervention: Greater Occipital Nerve Block with dexamethasone and lidocaine

Group G

Greater occipital nerve block (GONB) under ultrasound guidance with lidocaine and dexamethasone on the side of headache

Intervention: Greater Occipital Nerve Block with 0.9% saline

Group S

Greater occipital nerve block (GONB) under ultrasound guidance on the side of headache with 0.9% Saline (Placebo)

Intervention: Greater Occipital Nerve Block with dexamethasone and lidocaine

Group S

Greater occipital nerve block (GONB) under ultrasound guidance on the side of headache with 0.9% Saline (Placebo)

Intervention: Greater Occipital Nerve Block with 0.9% saline

Outcomes

Primary Outcomes

Analgesic efficacy

Time Frame: 12 weeks

Change in Pain score assessed on Numeric Rating Scale (NRS) which ranges from 0 to 10. 0 is no pain and 10 is maximum pain.

Secondary Outcomes

  • Headache days(12 weeks)

Study Sites (1)

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