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Clinical Trials/CTRI/2017/06/008847
CTRI/2017/06/008847
Recruiting
Phase 4

Real world Non-interventional Observational Study of Hydroxyzine hydrochloride in Chronic Pruritus

Dr Reddys Laboratories Ltd0 sites400 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: null- Chronic Pruritus
Sponsor
Dr Reddys Laboratories Ltd
Enrollment
400
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Pms

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Patients clinically diagnosed with chronic pruritus due to dermatological conditions where physician has taken decision to prescribe hydroxyzine hydrochloride.
  • 2\. Patients aged 18 years to 50 years who provide informed consent for data collection.
  • 3\. Patients of both sexes.

Exclusion Criteria

  • 1\. Patients with chronic pruritus due to systemic causes.
  • 2\. Patients with known hypersensitivity to hydroxyzine hydrochloride or any component of this medication.
  • 3\. Females who are pregnant or are lactating.
  • 4\. Patients on other CNS medications, or known neurological conditions.

Outcomes

Primary Outcomes

Not specified

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