Status:

COMPLETED

Low and High Dose Dextrose Prolotherapy in the Treatment of Lateral Epicondylitis

Lead Sponsor:

Ahi Evran University Education and Research Hospital

Conditions:

Lateral Epicondylitis

Eligibility:

All Genders

18-65 years

Phase:

PHASE4

Brief Summary

Lateral epicondylitis (tennis elbow) is an enthesopathy seen in 1-2% of the population aged 30-65 years, which can occur in the lateral epicondyle origo of the extensor carpi radialis brevis and longu...

Detailed Description

Lateral epicondylitis (tennis elbow) is an enthesopathy seen in 1-2% of the population aged 30-65 years, which can occur in the lateral epicondyle origo of the extensor carpi radialis brevis and longu...

Eligibility Criteria

Inclusion

  • Those who admit Kirsehir Ahi Evran University Hospital and is diagnosed with lateral epicondylitis,
  • Participants with unilateral or bilateral lateral epicondylitis and pain and functional limitations due to this condition,
  • who can read and write in Turkish,
  • participant's admission participating in the study,
  • participants who do not have exclusion criteria,

Exclusion

  • receiving any injection therapy to the elbow area in the last 3 months,
  • participants with complaints less than 3 months(acute lateral epicondylitis)
  • previously surgery on the elbow area,
  • having a history of acute trauma or fracture in the elbow area,
  • have local dermatological problems,
  • have a local infection in the treatment area,
  • those who are allergic to dextrose,
  • with coagulation disorders or using anticoagulant drugs,
  • with an autoimmune disease,
  • with type 1 or type 2 diabetes mellitus,
  • have unregulated hypertension,
  • have immune dysfunction,
  • with malignancy or diagnosed with a malignancy in the last 5 years,
  • pregnancy or lactation,
  • having cervical radiculopathy in the same extremity,
  • with cognitive dysfunction,
  • patients with paralysis in the same extremity,
  • lack of cooperation due to cognitive impairment,
  • participant's refusal to participate in the study.

Key Trial Info

Start Date :

January 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 21 2022

Estimated Enrollment :

75 Patients enrolled

Trial Details

Trial ID

NCT04680936

Start Date

January 1 2021

End Date

May 21 2022

Last Update

May 26 2022

Active Locations (1)

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Kirsehir Ahi Evran University Hospital

Kırşehir, Turkey (Türkiye)