Does Pre-injection Local Anesthesia Affect Experienced Pain During Intra-articular Hip Injections.

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

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-01-03

Study Completion Date

2022-01-02

Brief Summary

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Intra-articular hip injections are commonly used for diagnostic and therapeutic purposes but are often associated with patient anxiety and fear. The disparity between anticipated and experienced pain during these injections, as well as the role of pre-injection local anesthesia in pain modulation, remains unclear.

This study investigates the difference between anticipated and experienced pain during intra-articular hip injections. In addition, the study examines the impact of pre-injection local anesthesia in 60 prospectively recruited patients, some of whom received pre-injection local anesthesia while others did not. These study findings provide valuable insights into experienced pain during intra-articular hip injections, which can be applied to improve patient experiences and treatment compliance.

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Detailed Description

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1. Identification of patients in the outpatient clinic and completion of the questionnaires will be carried out by the principal investigator and sub-investigators in the clinic.
2. Data processing will be conducted by physicians holding an MD certification.
3. The type of study is prospective.
4. Data collection will be performed using the medical records of Tel Aviv Medical Center Hospital only, covering the years 2021 and 2022.
5. Demographic data will be collected, including gender, year of birth, age, diagnosis, indication for injection, and previous treatments. Clinical data will include underlying diseases, side of injection, complications, indications, and follow-up time.

Conditions

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Pain Injection Prevention Assessment

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Pre-injection superficial local anesthesia prior to Intra-articular corticosteroid injection

Intra-articular corticosteroid injection

Intervention Type PROCEDURE

Intra-articular hip injections with and without local anastesia and questionnaire about pain and anxiety related to the procedure was administered before and after the injection to the study and control groups.

Patients without pre-injection local anesthesia prior to Intra-articular corticosteroid injection

Intra-articular corticosteroid injection

Intervention Type PROCEDURE

Intra-articular hip injections with and without local anastesia and questionnaire about pain and anxiety related to the procedure was administered before and after the injection to the study and control groups.

Interventions

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Intra-articular corticosteroid injection

Intra-articular hip injections with and without local anastesia and questionnaire about pain and anxiety related to the procedure was administered before and after the injection to the study and control groups.

Intervention Type PROCEDURE

Other Intervention Names

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Local anasthesia

Eligibility Criteria

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Inclusion Criteria

* Patients undergoing a first-time intra-articular hip injection as indicated by an orthopedic surgeon.
* Indications for injection include:
* Diagnostic purposes (e.g., lidocaine test, arthrography)
* Therapeutic purposes (e.g., steroid injection for osteoarthritis)
* Participants must be 18 years of age or older.
* No previous hip joint injections.
* Ability to fill in the survey questionnaire.

Exclusion Criteria

* Patients under 18 years of age.
* Patients with a known history of hypersensitivity or allergy to the injectant material (e.g., local anesthetics, steroids).
* Patients lacking the ability to sign informed consent or complete a survey questionnaire.
* Patients with previous hip joint injections, due to the potential for recalling prior pain experienced.

Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No