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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01651338
Other study ID # accupuncture
Secondary ID iaum
Status Terminated
Phase Phase 2/Phase 3
First received July 17, 2012
Last updated July 25, 2012
Start date January 2009
Est. completion date January 2010

Study information

Verified date July 2012
Source Islamic Azad University, Tehran
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

Chronic pains can affect the life quality. This study has performed in the first time in Mashhad.The purpose of the present study was to examine the effect of acupuncture on the life quality of 150 patients who suffered from chronic pain. Some people like performing acupuncture because they believed it's free of risks and beneficial.

In order to achieve this purpose, we had examined the life quality of the patients before and after acupuncture. This study was randomly performed on 150 patients aged between 17-75. They were suffering from chronic pain.

The questionnaire is based on WHO QOL. The questionnaires were filled out once before acupuncture and once 12 weeks after it.


Description:

This study was completed on time.


Recruitment information / eligibility

Status Terminated
Enrollment 150
Est. completion date January 2010
Est. primary completion date August 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 17 Years to 75 Years
Eligibility Inclusion Criteria:

- aged between 17 - 75 years old,

- suffering from arthritis pains,

- migraine backaches,

- muscular spasms,

- pains in the neck, and in the knee

- duration of disease over 1 year

Exclusion Criteria:

- tacking pain relief

- pregnant women

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Procedure:
acupuncture
The patients went through acupuncture for 8 -10 sessions and either once or two times a week. The number and the place of needles were 8 -12 for each patient which were located on the right place.

Locations

Country Name City State
Iran, Islamic Republic of Dr sadre Nabavi clinic Mashhad Khorasane Razavi

Sponsors (1)

Lead Sponsor Collaborator
Islamic Azad University, Tehran

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary quality of life improvement up to 3 months No
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