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Ibuprofen Sodium Tension Headache Study

Pfizer logo

Pfizer

Status and phase

Completed
Phase 3

Conditions

Pain

Treatments

Drug: Ibuprofen Sodium
Drug: Standard Ibuprofen
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT01362491
B3411007
AH-11-16

Details and patient eligibility

About

This study will compare the ability of a single-dose of a novel ibuprofen formulation to relieve pain compared to placebo and standard ibuprofen in the treatment of tension-type headache

Enrollment

226 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males and females at least 18 years to 65 years of age
  • A diagnosis of an episodic tension-type headache, as defined by the International Headache Society

Exclusion criteria

  • Pregnancy or breast-feeding
  • Alcohol or substance abuse
  • Any serious medical or psychiatric disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

226 participants in 3 patient groups, including a placebo group

Treatment A
Experimental group
Treatment:
Drug: Ibuprofen Sodium
Treatment B
Active Comparator group
Treatment:
Drug: Standard Ibuprofen
Treatment C
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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