The Effect of Panax Notoginseng Powders on Rheumatic Pain

NCT ID: NCT02260336

Last Updated: 2017-04-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2018-12-31

Brief Summary

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The purpose of this study is to evaluate the effect of Panax Notoginseng Powders on Rheumatic Pain.

Detailed Description

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Conditions

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Rheumatic Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Panax Notoginseng Powder 1g

Panax Notoginseng Powder 1g, daily

Group Type EXPERIMENTAL

Panax Notoginseng Powder 1g

Intervention Type DIETARY_SUPPLEMENT

Panax Notoginseng Powder 5g

Panax Notoginseng Powder 5g,daily

Group Type EXPERIMENTAL

Panax Notoginseng Powder 5g

Intervention Type DIETARY_SUPPLEMENT

Panax Notoginseng Powder 10g

Panax Notoginseng Powder 10g,daily

Group Type EXPERIMENTAL

Panax Notoginseng Powder 10g

Intervention Type DIETARY_SUPPLEMENT

Panax Notoginseng Powder 15g

Panax Notoginseng Powder 15g,daily

Group Type EXPERIMENTAL

Panax Notoginseng Powder 15g

Intervention Type DIETARY_SUPPLEMENT

Celecoxib Capsule 400 mg daily

Celecoxib Capsule 400 mg daily

Group Type ACTIVE_COMPARATOR

Celecoxib Capsule 400 mg daily

Intervention Type DRUG

Interventions

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Panax Notoginseng Powder 1g

Intervention Type DIETARY_SUPPLEMENT

Panax Notoginseng Powder 5g

Intervention Type DIETARY_SUPPLEMENT

Panax Notoginseng Powder 10g

Intervention Type DIETARY_SUPPLEMENT

Panax Notoginseng Powder 15g

Intervention Type DIETARY_SUPPLEMENT

Celecoxib Capsule 400 mg daily

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* had a diagnosis of classic or definite RA
* without conflict to the written, informed consent signed prior to the enrollment.

Exclusion Criteria

* uncontrolled medical problems
* organic brain syndrome
* major psychiatric disturbances
* major communicative disorders
* a history of severe noncompliance
* less than 7 years of formal education, or illiteracy
* being included in other clinical trial within the last 4 weeks
* with abnormal liver or kidney function (more than 1 time above the high normal)
* with serious cardiovascular disease
* with hematologic disease
* being in pregnancy, lactation period or under a pregnancy plan
* with severe gastrointestinal disease
* with contraindication or being allergic to the test drugs
* being under the treatment of drugs within 1 previous week, that might affect the results of the trial, such as non-steroidal anti-inflammatory drugs
* being not compatible for the trial medication, or other circumstances at the discretion of investigators
* without legal capacity or only with limited legal capacity
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chengdu PLA General Hospital

OTHER

Sponsor Role lead

Responsible Party

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Yang Min

Ph.D

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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270 Rongdu street, Jin-niu district,Rheumatology Center of Integrated Medicine, General Hospital of Chengdu Military Area Command PLA,

Chengdu, Sichuan, China

Site Status

Countries

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China

Other Identifiers

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PNP01RP001

Identifier Type: -

Identifier Source: org_study_id

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