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Evaluation of the efficacy of behavioral remodeling for treatment of resistant pes anserine tendino-bursitis

Evaluation of the efficacy of behavioral remodeling for treatment of resistant pes anserine tendino-bursitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017031112823N4
Enrollment
60
Registered
2017-08-22
Start date
2017-07-23
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

Pes anserine bursitis. Other bursitis of knee

Interventions

Intervention 1: In intervention group, in addition to receive naproxen (500 mg q 12 hrs) or diclofenac (75 mg per day) and pantoprazole (40 mg per day) for 2 weeks, weight loss, avoid to kneeling down
Behavior
In intervention group, in addition to receive naproxen (500 mg q 12 hrs) or diclofenac (75 mg per day) and pantoprazole (40 mg per day) for 2 weeks, weight loss, avoid to kneeling down and sitting cro
In control group, patients receive naproxen (500 mg q 12 hrs) or diclofenac (75 mg per day) and pantoprazole (40 mg per day) for 2 weeks, weight loss, avoid to kneeling down and sitting crossed leg, q

Sponsors

Semnan University of Medical Sciences, Vice Chancellor for Research and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 50 to 60 years old female with BMI=25 - 30 kg/m2 Exclusion criteria : Patient with cardiac disease, Diabetes, HTN , Peptic ulcer and duodenal ulcer, Cancer , Hepatic and Renal disorder , analgesic drugs intolerance , previous knee surgery or trauma or RA and previous treatment of PATB during last year

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of pain. Timepoint: Befor intervantion , 2 months after intervention. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Body mass index. Timepoint: Befor intervantion , 2 months after intervention. Method of measurement: weight/(height)2.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJamileh Moghimi

Semnan University of Medical Sciences

are20935@gmail.com+98 23 3345 1336

Outcome results

None listed

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