Dexamethasone Plus Metoclopramide Versus Paracetamol/NSAIDs for Primary Headache

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-60
SponsorPak Emirates Military Hospital

About this trial

Primary headache disorders are among the most common neurological conditions presenting to emergency departments and can significantly impair quality of life and daily functioning. Various medications are used for acute headache treatment, including paracetamol, non-steroidal anti-inflammatory drugs (NSAIDs), metoclopramide, and corticosteroids.

This randomized controlled trial aims to compare the efficacy of intravenous dexamethasone combined with metoclopramide versus intravenous paracetamol/NSAIDs in patients presenting with primary headache to the emergency department of Pak Emirates Military Hospital, Rawalpindi.

A total of 94 patients aged 18 to 60 years with clinically diagnosed primary headache will be enrolled and randomized into two groups. Group A will receive intravenous dexamethasone 8 mg plus intravenous metoclopramide 10 mg, while Group B will receive intravenous paracetamol or NSAIDs according to departmental protocol. Pain severity will be assessed using the Visual Analogue Scale (VAS) before treatment and again after 60 minutes. Treatment efficacy will be defined as at least 50% reduction in pain score from baseline.

The results of this study may help identify a more effective treatment strategy for acute primary headache management in emergency departments.

Eligibility criteria

Qualifiers

Patients aged 18 to 60 years.

Patients presenting with primary headache diagnosed clinically.

Patients presenting within 72 hours of onset of headache.

Patients with Visual Analogue Scale (VAS) pain score ≥5.

Disqualifiers

Patients with secondary headache disorders.

Patients with known allergy to dexamethasone, metoclopramide, paracetamol, or NSAIDs.

Pregnant females.

Patients with hepatic impairment.

Trial design

Treatments tested in this trial

  • Dexamethasone Plus Metoclopramide
  • Paracetamol/NSAIDs

Treatment groups

94 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators