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The effect of acupressure in the treatment of carpal tunnel syndrome

The effect of acupressure on the clinical manifestations of Carpal Tunnel Syndrome (CTS)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201609178717N4
Enrollment
60
Registered
2016-10-24
Start date
2016-10-22
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: The first intervention (the use of acupressure): In this group, acupressure is performed for a period of one month. For applying acupressure, the Sea-Band button is placed at all times
Treatment - Other
Placebo
The first intervention (the use of acupressure): In this group, acupressure is performed for a period of one month. For applying acupressure, the Sea-Band button is placed at all times day and night o
The second intervention (the use of the placebo): In this group, the placebo will be used for one month. For applying placebo, the Sea-Band button is placed at all times day and night on the external
Third intervention (routine treatment in control group): People in this group, only the routine treatment (splint and analgesic drugs) will receive. Boston Carpal Tunnel Questionnaire (BCTQ) to evalua

Sponsors

Vice chancellor for research of Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The age of patients is 20-70 years; Carpal tunnel syndrome be diagnosed by orthopedic specialist; Symptoms lasting more than 3 months; Having no skin problem at the close Sea-Band site. Exclusion criteria: Patients with a history of wrist or median nerve trauma; CTS that are followed pregnancy, alcoholism, systemic diseases; Patients with a history of stroke and cerebral palsy; Illiterate Patients; Obese patients; Patients with a low level of consciousness; Patients who due to intensity of disease symptoms in during the study, surgical treatment or corticosteroid injections be necessary; Patients who can not tolerate Sea-Band.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Distal sensory latency (DSL). Timepoint: Before the intervention in the first session and after the intervention (after a month. Method of measurement: By EMG device.;Nerve conduction velocity (NCV). Timepoint: Before the intervention in the first session and after the intervention (after a month). Method of measurement: By EMG device.;Hand muscle strength (Grip power). Timepoint: Before the intervention in the first session and after the intervention (after a month). Method of measurement: By hand-held dynamometer device.;Clinical manifestations of Carpal Tunnel Syndrome (CTS). Timepoint: Before the intervention in the first session and after the intervention (after a month). Method of measurement: By Boston Carpal Tunnel Questionnaire (BCTQ).;Pinch power. Timepoint: Before the intervention in the first session and after the intervention (after a month). Method of measurement: by Digital dynamometer Device.;Distal motor latency (DML). Timepoint: Before the intervention in the first session and after the intervention (after a month). Method of measurement: By EMG device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammad Reza Asgari

Semnan University of Medical Sciences

asgari5000@gmail.com+98 23 3344 0758

Outcome results

None listed

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