Evaluation of the Effectiveness of Genicular Block in Postoperative Analgesia in Patients Undergoing Knee Arthroscopy

May 15, 2024 updated by: Sevil Azazoglu ERBEK, Başakşehir Çam & Sakura City Hospital
The effectiveness of genicular block in postoperative analgesia management in arthroscopy cases are intended to be evaluated.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Relieving postoperative arthroscopy pain requires multimodal approaches of pain The most common treatment options are nonsteroidal anti-inflammatory drugs (NSAIDs), opioids and local infiltration of anesthetics is used. Due to the side effects of NSAIDs and opioids application of regional analgesia techniques, while providing better analgesia quality.

It can reduce complications . Peripheral blocks such as genicular block, reduce side effects by reducing the use of other analgesics . Pain, it is considered one of the most important factors affecting the quality of recovery.

Study Type

Observational

Enrollment (Estimated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Our patients who will be included in the research are patients who underwent arthroscopy under elective conditions.

It consists of volunteers over the age of 18, regardless of gender.

-

Description

Inclusion Criteria:

Our patients who will be included in the research are patients who underwent arthroscopy under elective conditions.

It consists of volunteers over the age of 18, regardless of gender.

-

Exclusion Criteria:

  • Infection in the block area
  • Coagulation disorder,
  • Known allergy to local anesthetics
  • Pregnancy
  • Patient with neuropathy
  • Uncooperative patient
  • The patient who refused to participate in the study
  • Patients under 18 years of age

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
the perioperative effect of genicular block
Time Frame: 06.10.2024-12.10.2024

The primary implication of this study is the perioperative effect of genicular block in arthroscopy surgery.

To show that it has sufficient contribution to multimodal analgesia.
06.10.2024-12.10.2024

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Başakşehir Çam & Sakura City Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

June 10, 2024

Primary Completion (Estimated)

December 10, 2024

Study Completion (Estimated)

December 10, 2024

Study Registration Dates

First Submitted

May 9, 2024

First Submitted That Met QC Criteria

May 13, 2024

First Posted (Actual)

May 14, 2024

Study Record Updates

Last Update Posted (Actual)

May 16, 2024

Last Update Submitted That Met QC Criteria

May 15, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2024-296

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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