IPICK Blocking for TKA With Moderate Flexion Contracture
NCT ID: NCT04603950
Last Updated: 2022-07-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
42 participants
INTERVENTIONAL
2020-11-01
2021-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
A New Technique to Produce Anatomical Alignment Results With Less Midflexion Instability in Total Knee Arthroplasty
NCT02450409
Tourniquet Application on Total Knee Arthroplasty
NCT03256058
A Study on the Use of Tourniquet Use In Primary Total Knee Arthroplasty
NCT04502459
Comparison of High Flex and Standard Rotating Platform Total Knee Arthroplasty (TKA)
NCT01176292
How Total Knee Prosthesis Dessigns Influence in Quality of Live
NCT02050438
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
study group
The first 20 patients received Continue Adductor Canal Block + Infiltration between the Popliteal Artery and Capsule of the Knee
CACB+IPACK
continue adductor canal block plus Infiltration between the Popliteal Artery and Capsule of the Knee
control group
The second 20 patients received Continue Adductor Canal Block alone
CACB
continue adductor canal block
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
CACB+IPACK
continue adductor canal block plus Infiltration between the Popliteal Artery and Capsule of the Knee
CACB
continue adductor canal block
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. The flexion contracture was between 5 and 10 degrees
3. ASA grade I-III
Exclusion Criteria
2. Contraindications of nerve anesthesia or regional anesthesia.
3. unable to cooperate, allergic to the drugs used in this study.
4. Non steroidal anti-inflammatory drugs are not tolerated.
5. chronic opioid consumption (daily or almost daily use)
50 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
The First Hospital of Jilin University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The First Hospital of Jilin University
Changchun, , China
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
QiXin2
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.