Proximal, Mid, and Distal Adductor Canal Block for Pain Control After Total Knee Arthroplasty
NCT07926373, Not applicable, Not yet recruiting, Bursa City Hospital
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Proximal, Mid, and Distal Adductor Canal Block for Pain Control After Total Knee Arthroplasty | ClinicalTrials.gov |
| NCT number | NCT07926373 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 120 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Bursa City Hospital | ClinicalTrials.gov |
| Conditions | Postoperative Pain, Arthroplasty, Replacement, Knee, Knee Osteoarthritis | ClinicalTrials.gov |
| Interventions | Proximal Adductor Canal Block, Mid Adductor Canal Block, Distal Adductor Canal Block | ClinicalTrials.gov |
| First posted | 2026-11-09 | ClinicalTrials.gov |
| Last updated | 2026-11-09 | ClinicalTrials.gov |
Registered outcomes 5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Total Tramadol Consumption in the First 24 Hours | Postoperative 0-24 hours | Cumulative tramadol consumption (mg) delivered via patient-controlled analgesia (PCA) during the first 24 hours after surgery. | ClinicalTrials.gov |
| Secondary | Pain Scores at Rest | Postoperative 0, 1, 2, 4, 8, 12, 24, and 48 hours | Pain at rest assessed with the Numeric Rating Scale (NRS; 0 = no pain, 10 = worst imaginable pain). | ClinicalTrials.gov |
| Secondary | Pain Scores During Movement | Postoperative 0, 1, 2, 4, 8, 12, 24, and 48 hours | Pain during standardized knee flexion or active/passive movement assessed with the NRS (0-10). | ClinicalTrials.gov |
| Secondary | Tramadol Consumption at Predefined Intervals | Postoperative 0-48 hours | PCA tramadol consumption (mg) in the 0-4, 4-8, 8-24, and 24-48 hour intervals and cumulative 48-hour consumption. | ClinicalTrials.gov |
| Secondary | Time to First Rescue Analgesic Request | Postoperative 0-48 hours | Time (minutes) from the end of surgery to the first administration of rescue analgesia (meperidine 50 mg), given when NRS is 4 or higher or analgesia is inadequate despite PCA. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)