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Efficacy of topical linseed oil on patients with pregnancy-related carpal tunnel syndrome

Efficacy of topical linseed oil on patients with pregnancy-related carpal tunnel syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015110224832N1
Enrollment
60
Registered
2015-11-27
Start date
2015-12-22
Completion date
Unknown
Last updated
2018-02-22

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: Linseed oil products,with the size of a pea (depending on the size of the patient, so that the area is completely covered) and 3 times a day (morning, afternoon and night), for use in
Treatment - Drugs
Placebo
Linseed oil products,with the size of a pea (depending on the size of the patient, so that the area is completely covered) and 3 times a day (morning, afternoon and night), for use in wrist palmar are
Base of moisturizing gel, with the size of a pea (depending on the size of the patient, so that the area is completely covered) and 3 times a day (morning, afternoon and night), for use in wrist palma

Sponsors

Fasa University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: nclusion criteria: pregnancy-related carpal tunnel syndrome; patients aged between 18-45 years old; electrodiagnostic criteria for mild to severe CTS; patient's written informed consent for inclusion; having at least two signs or one sign plus one symptom of: paresthesias, numbness, tingling, night pain positive Phalen test, positive Tinnel test, positive compression test. Exclusion criteria: recurrent carpal tunnel syndrome; positive history of trauma and/or fracture of wrist bones and/or surgical release of median nerve and/or direct injection into carpal tunnel of wrist; evidence of cervical radiculopathy in EMG; systemic disease including: neuropathies (rule out by nerve conduction study of ulnar nerves) and/or collagen vascular diseases such as SLE and scleroderma and RA; endocrine diseases such as hypothyroidism and DM; other disease-inducing neuropathy; situations such as renal failure and/or alcoholism and/or poor medical condition; History of recent and ongoing use of corticosteroids or analgesics that could not be discontinued; hypersensitivity to the drug or placebo; inability to completion of data gathering forms (cognitive or language disorder).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Boston Carpal Tunnel Questionnaire score. Timepoint: At the beginning of the study and after 4 weeks. Method of measurement: Boston Carpal Tunnel Questionnaire.

Secondary

MeasureTime frame
Median nerve sensory distal latency. Timepoint: At the beginning of the study and after 4 weeks. Method of measurement: Electrodiagnosis.;Median nerve wrist sensory nerve conduction velocity. Timepoint: At the beginning of the study and after 4 weeks. Method of measurement: Electrodiagnosis.;Median nerve motor distal latency. Timepoint: At the beginning of the study and after 4 weeks. Method of measurement: Electrodiagnosis.;Median nerve compound latency. Timepoint: At the beginning of the study and after 4 weeks. Method of measurement: Electrodiagnosis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Alireza Askari

Fasa University of Medical Sciences

aaskari@yahoo.com+98 71 5335 0994

Outcome results

None listed

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