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Effect of Frankincense on carpal tunnel syndrome

Evaluation the effectiveness of Frankincense on symptoms,signs & electrodiagnostic parameters of patients with carpal tunnel syndrome.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180731040647N1
Enrollment
36
Registered
2019-02-24
Start date
2018-11-06
Completion date
Unknown
Last updated
2019-03-25

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

Conditions

carpal tunnel syndrome. Mononeuropathies of upper limb,urrent traumatic nerve disorder,Carpal tunnel syndrome

Interventions

Intervention 1: Intervention group: they go under treatment of topical product,derived from Frankincense ,every other 12 hours for 6 weeks on their volar surface of wrist.they also wear cock up splint

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients aged >=18 years Patients with unilateral or bilateral mild or moderate CTS Patients who heve at least two signs or one sign and one symptom of CTS, such as numbness, paresthesia, positive Tinel or Phalen tests patients who agreed to participate in this study

Exclusion criteria

Exclusion criteria: Patients with severe CTS Patients with history of previous surgical release of the median nerve Patients with sequelae of fracture of the wrist Patient who have intra canal corticosteroids injection in the last 6 months Patients with cervical radiculopathy Patient who have taken analgesics or cortcosteroid Patients with any undelying disease such as DM, CRF, neuropathy Alcoholic patients Patients who have allergy to drug or placebo Patients who do not agree to participate or who do not sign the consent form

Design outcomes

Primary

MeasureTime frame
Pain score based on visual analogue scale. Timepoint: Before intervention and 2,6 weeks after intervention. Method of measurement: Visual Analogue Scale.;Grip power in affected hand. Timepoint: Before intervention and 2 and 6 weeks after intervention. Method of measurement: hand dynamometry.;Electrodiagnostic parameters including median sensory and motor nerve conduction studies to determine initial latency and base to peak amplitude are registered. Timepoint: Before intervention and 2,6 weeks after intervention. Method of measurement: Electrodiagnostic machine.;Symptom severity scale & functional status scale. Timepoint: Before intervention and 2,6 weeks after intervention. Method of measurement: Boston Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSetareh Rohani Shahraki

Tehran University of Medical Sciences

setarehhhr87@gmail.com+98 21 4464 0337

Outcome results

None listed

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