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ALGRX 4975 in the Treatment of Tennis Elbow

Primary Purpose

Tennis Elbow

Status
Completed
Phase
Phase 2
Locations
Slovakia
Study Type
Interventional
Intervention
ALGRX 4975
Sponsored by
AlgoRx Pharmaceuticals
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tennis Elbow focused on measuring Acute lateral epicondylitis, Tennis elbow, Capsaicin

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Acute lateral epicondylitis (LE) of less than 3 months duration (subjects with recurrent acute LE may be included). A screening and baseline severity of pain on resisted wrist dorsiflexion score of moderate or greater intensity. Lidocaine responsive. A systolic and diastolic blood pressure not greater than 140 and 95 mm Hg, respectively. Exclusion Criteria: Any clinically significant form of joint disease, elbow trauma or neuromuscular disorder at the elbow, other than acute LE. Physiotherapy treatment within the preceding 2 weeks, prior to Visit 1. Any systemic or local corticosteroids within the preceding 3 months, except nasal or inhaled steroids at less than or equal to 1000 mcg/day. A medical condition other than LE that requires the use of a pain medication. A peripheral sensory or motor neuropathy involving the upper extremities.

Sites / Locations

  • Ortopedicko-Traumatologicka Klinika

Outcomes

Primary Outcome Measures

Pain induced by resisted wrist dorsiflexion 4 weeks after treatment

Secondary Outcome Measures

Pain induced by resisted wrist dorsiflexion (other than 4 weeks)
Grip strength
Pain experienced during the grip strength test
Pain in elbow over previous 24 hours
Effect on work
Tenderness elicited by investigator or designee
Subjects' global impression of change
Secondary outcomes are evaluated at 1, 2, 4, 8 and 12 weeks.

Full Information

First Posted
August 15, 2005
Last Updated
December 18, 2006
Sponsor
AlgoRx Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00130949
Brief Title
ALGRX 4975 in the Treatment of Tennis Elbow
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Phase II, Exploratory Evaluation of ALGRX 4975 in Subjects With Acute Lateral Epicondylitis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
November 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
AlgoRx Pharmaceuticals

4. Oversight

5. Study Description

Brief Summary
Tennis elbow is a painful condition that results from repetitive arm movement with overuse of muscles, e.g. when playing tennis. A single injection of ALGRX 4975 has the potential to reduce pain for a period of weeks to months. This study will test the efficacy and safety of ALGRX 4975 in the treatment of patients with tennis elbow.
Detailed Description
Lateral epicondylitis (tennis elbow) is a painful condition that affects 4 to 7 adults per 1000 annually and tends to involve the subject's dominant side. It typically results from repetitive arm movement with over use of muscles leading to small tears in the tendons attaching muscles of the forearm to the epicondyles that may progress to tendonitis. Pain on or around the lateral epicondyle may radiate down the subject's arm. Gripping or extending the wrist often intensifies the pain. More than 40 possible treatments have been proposed, reflecting a lack of consensus about optimal management. Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to treat tennis elbow, but there are no trials to date that have compared them with other painkillers and one study found no clinically important benefit over placebo. Use of corticosteroid injections provides mixed results in relief of pain and at times insufficient evidence to support their use. Although complications associated with steroid injection are relatively uncommon, when a complication does occur, it can result in severe and disabling consequences for the subject. A small proportion of subjects fail to respond to only one injection of corticosteroid and some subjects who initially improved at four weeks had worse symptoms by six months. This study has been designed to evaluate the safety and efficacy of a single soft tissue injection of ALGRX 4975 at a dose of 100 µg in comparison to placebo in subjects with acute LE.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tennis Elbow
Keywords
Acute lateral epicondylitis, Tennis elbow, Capsaicin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
45 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
ALGRX 4975
Primary Outcome Measure Information:
Title
Pain induced by resisted wrist dorsiflexion 4 weeks after treatment
Secondary Outcome Measure Information:
Title
Pain induced by resisted wrist dorsiflexion (other than 4 weeks)
Title
Grip strength
Title
Pain experienced during the grip strength test
Title
Pain in elbow over previous 24 hours
Title
Effect on work
Title
Tenderness elicited by investigator or designee
Title
Subjects' global impression of change
Title
Secondary outcomes are evaluated at 1, 2, 4, 8 and 12 weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute lateral epicondylitis (LE) of less than 3 months duration (subjects with recurrent acute LE may be included). A screening and baseline severity of pain on resisted wrist dorsiflexion score of moderate or greater intensity. Lidocaine responsive. A systolic and diastolic blood pressure not greater than 140 and 95 mm Hg, respectively. Exclusion Criteria: Any clinically significant form of joint disease, elbow trauma or neuromuscular disorder at the elbow, other than acute LE. Physiotherapy treatment within the preceding 2 weeks, prior to Visit 1. Any systemic or local corticosteroids within the preceding 3 months, except nasal or inhaled steroids at less than or equal to 1000 mcg/day. A medical condition other than LE that requires the use of a pain medication. A peripheral sensory or motor neuropathy involving the upper extremities.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gabriel Vasko, MD PhD
Organizational Affiliation
Ortopedicko-Traumatologicka Klinika, Kosice, Slovak Republic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ortopedicko-Traumatologicka Klinika
City
Kosice
ZIP/Postal Code
040 11
Country
Slovakia

12. IPD Sharing Statement

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ALGRX 4975 in the Treatment of Tennis Elbow

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