Overview

Gabapentin - A Solution to Uremic Pruritus?

Status:
Unknown status
Trial end date:
2006-03-01
Target enrollment:
0
Participant gender:
All
Summary
To investigate using the drug gabapentin to relieve the intense pruritic sensation associated with chronic renal failure patients undergoing peritoneal dialysis.
Phase:
N/A
Details
Lead Sponsor:
Hospital Authority, Hong Kong
Collaborator:
Pfizer
Treatments:
Gabapentin
gamma-Aminobutyric Acid
Criteria
Inclusion Criteria:

- Adult Chinese male and female patients aged > 18 undergoing CAPD for at least 3 months
and able to read and understand Chinese

- Patients experiencing moderate to severe pruritis, defined as persistent,
treatment-resistant pruritis considerably impairing sleep or daytime activity.
Treatment resistance is defined as no or only partial resolvement of pruritis under
current anti-pruritis treatment regimens such as anti-pruritis lotions and
anti-histamines.

- Patients in stable clinical condition in terms of peritoneal dialysis and general
health

- Patients able to understand and answer the SDS questionnaire

- Patients able to express the sensation of itchiness in the terms of the VAS and the
SDS score

- Patients who are willing to give written informed consent and to participate in and
comply with the study protocol

Exclusion Criteria:

- Patients with a known history of pruritis or dermatologic disease antedating renal
failure.

- Patients with skin disease other than the usual cutaneous findings of uraemia such as
xerosis or ecchymosis.

- Patients under current treatment with systemic steroids

- Known history of allergy to Gabapentin

- Those patients already put on anti-convulsants

- Unable to give written informed consent for the study

- Pregnancy or female patients of child-bearing age who are unwilling to use
contraception

- Poor drug compliance

- Known HIV positivity

- Active neoplastic disease

- Those who do not want to participate the study