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Evaluation of Clemastine effects in CTS pateints

Evaluation of Clemastine effects on clinical and electrodiagnostic parameters in Carpal tunnel syndrome (CTS) patients: A double blind RCT

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190428043404N2
Enrollment
20
Registered
2023-04-23
Start date
2023-05-22
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Carpal tunnel syndrome. Carpal tunnel syndrome

Interventions

Intervention 1: Intervention group: 1 mg clemastine tablet every night along with CTS night splint (Volar cockup wrist splint, Prefabricated) for three months. Intervention 2: Control group: Taking a

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Pain or paresthesia or hypoesthesia in distal hand region or thenar weakness, with positive tinel or phalen tests No clinical evidence of cervical radiculopathy or radicular pain Negative history for Carpal Tunnel Release (CTR) surgery No injection inside or in proximity of carpal tunnel in last 3 months No present contraindication for Clemastine, such as drug allergy to antihistamine group Patient is willing to knowingly participate in a clinical trial

Exclusion criteria

Exclusion criteria: Patient isn't cooperative for questionnaire completion Drug or alcohol addiction Major depressive disorder or uncontrolled psychiatric disorders Positive history for malignancy or infection in wrist or hand region History of ischemic or neurovascular injury in wrist or hand region Usage of other treatment measures during trial period Patient doesn't follow correct treatment plan regarding drug or splint usage

Design outcomes

Primary

MeasureTime frame
Patient's pain intensity(Visual Analogue Scale). Timepoint: Before, after one month and after three months of intervention. Method of measurement: Using the Visual Analogue Scale.;Median nerve sensory action potential amplitude. Timepoint: Before, after one month and after three months of intervention. Method of measurement: Nerve conduction study.;Median nerve sensory action potential latency. Timepoint: Before, after one month and after three months of intervention. Method of measurement: Nerve conduction study.;Median nerve motor action potential latency. Timepoint: Before, after one month and after three months of intervention. Method of measurement: Nerve conduction study.;Median nerve motor action potential amplitude. Timepoint: Before, after one month and after three months of intervention. Method of measurement: Nerve conduction study.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGolam Reza Raissi

Iran University of Medical Sciences

raissi.gh@iums.ac.ir+98 21 8214 1612

Outcome results

None listed

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