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Continuous Adductor Canal Block for Total Knee Arthroplasty Analgesia

Prospective Comparison Between Continuous Femoral Nerve Block and the Association of Adductor Canal Block and Sciatic Nerve Block in Total Knee Arthroplasty.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02387021
Enrollment
80
Registered
2015-03-12
Start date
2015-03-31
Completion date
2015-12-31
Last updated
2015-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuromuscular Blockade, Pain Management

Keywords

analgesia, nerve block, Total knee replacement

Brief summary

The purpose of the study is to determine whether the association of sciatic nerve block to continuous adductor canal block is effective in the treatment of total knee arthroplasty post operative pain .

Interventions

PROCEDUREinfragluteal Sciatic nerve block
DRUGSaline

Sponsors

Institut Kassab d'Orthopédie
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Elective unilateral TKA, * Planned continuous spinal anesthesia , * Ability to follow study protocol, * American Society of Anesthesiologists class 1 to 3.

Exclusion criteria

* Contraindication for neuraxial anesthetic, * Chronic opioid use (defined as daily or almost daily use of opioids for \>3 months), * Hypersensitivity and/or allergies to any of the study medications, * Intraoperative use of volatile anesthetics, * Preexisting neuropathy on the operative limb, * Contraindications to a femoral, adductor canal or Tibial nerve block.

Design outcomes

Primary

MeasureTime frameDescription
Total Opioid-consumption8 hours postoperativeCumulative opioid consumption : converting oral, intravenous, and patient-controlled analgesia PCA opioid to morphine equivalent

Secondary

MeasureTime frameDescription
NRS pain score during movement0,1,2,4,6,8,12,24 and 48 hours postoperativeNRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale, during physiotherapy.
NRS pain score after 10 meters of walk or maximum walked distance8, 24 and 48 hours postoperativeNRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale after 10 meters walk (if enable after maximum walked distance).
Ability to walk8, 24 and 48 hours postoperativeThe ability of the patient to stand up and walk 3 meters.
NRS pain score at rest0,1,2,4,6,8,12,24 and 48 hours postoperativeNRS pain scores determined by patient interview, using the standard NRS of 0 to 10 scale at rest.
The 10-m walk test8, 24 and 48 hours postoperativetime it takes the patient to walk a distance of 10 m as quickly as possible
patient satisfaction8, 24 and 48 hours postoperativepatient interviewed, using a scale of 0-10, 0 not satisfied and 10 being the most satisfied
TUG Test8, 24 and 48 hours postoperativeThe TUG test measures the time it takes a patient to stand up from a chair, walk a distance of 3 m, and return to the chair

Contacts

Primary ContactKarim Raies, M.D
karim.raies@gmail.com+21655208602

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026