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The clinical study of effect of pregabalin to functional Magnetic Resonance Imaging (fMRI) and Iowa Gambling task (IGT) in postherpetic neuralgia patients

The clinical study of effect of pregabalin to functional Magnetic Resonance Imaging (fMRI) and Iowa Gambling task (IGT) in postherpetic neuralgia patients: a prospective, double blind, randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN55574777
Enrollment
40
Registered
2011-10-28
Start date
2011-12-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Postherpetic neuralgia Nervous System Diseases Postzoster neuralgia

Interventions

PHN patients were randomized to receive pregabalin 150mg twice a day (Bid) or placebo for 2 weeks. Rescue medication: Oxycodone 5-30mg/day or more orally was used as rescue medication for pain contro

Sponsors

Xinhua Hospital (China)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age greater than 60 years and over 40kg of body weight 2. Pain history is longer than 3 months 3. Pain on Visual Analogue Scale (VAS) >3 (0-10 VAS scale), the frequency of acute pain flares occurred more than 3 times per day 4. Refractory to formal treatment such as antiepileptic medicine, antidepressants, opioids and physical treatments and epidural block 5. No history of severe liver and renal diseases

Exclusion criteria

Exclusion criteria: 1. Withdraws from the study 2. Poor effect, intolerant to the study 3. Uncooperative and unable to finish the self evaluation (VAS, qulaity of life [QOL] and SF-36) 4. Coagulation disturbances 5. Allergies to drug 6. Malignancy

Design outcomes

Primary

MeasureTime frame
1. fMRI signal change, IGT results at baseline, days 14 after treatment 2. Visual Analogue Scale (VAS), measured at baseline, days1, 2, 3,7,14 after treatment 3. Flare pain per day during days 3, 7, 14 after treatment

Secondary

MeasureTime frame
1. SF-36 at baseline, days 14 after treatment 2. Dosage of rescue drug (Oxycodone) consumed per day at days3, 7, and 14 after treatment 3. Presence, frequency and duration of adverse effects at 7, 14 days

Countries

China

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026