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A new combined treatment for post-concussion syndrome: a pilot trial

Not Applicable
Conditions
Post-concussion syndrome
Mental and Behavioural Disorders
Postconcussional syndrome
Registration Number
ISRCTN45733939
Lead Sponsor
Durham University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
18
Inclusion Criteria

1. PCS patients, aged 18 to 64 years. PCS is defined as the persistence of concussion symptoms, for more than 3 months after the initial concussion event
2. Current PCS confirmed by the presence of more than three symptoms on the Rivermead PCS
3. Not using any other pharmaceutical treatment for the management of PCS, e.g. antidepressants
4. Can provide signed informed consent

Exclusion Criteria

1. Pregnancy
2. Breastfeeding
3. Hepatic insufficiency
4. Renal impairment
5. Any of the following BNF contraindications for cinnarizine: acute porphyrias; epilepsy; Parkinson's disease; prostatic hypertrophy; pyloroduodenal obstruction; susceptibility to angle-closure glaucoma; urinary retention
6. Any of the following BNF contraindications for piracetam: gastric ulcer; history of haemorrhagic stroke; increased risk of bleeding; recent or planned major surgery; underlying disorders of haemostasis; cerebral haemorrhage; Huntington's chorea

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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