Trial · NCT06112548
The Efficiency of Periarticular Multimodal Drug Injection in Pain Management Following Primary Unilateral TKA
NCT06112548, Not applicable, Completed, Damascus University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Efficiency of Periarticular Multimodal Drug Injection in Pain Management Following Primary Unilateral TKA. Trials, record NCT06112548. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06112548
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Efficiency of Periarticular Multimodal Drug Injection in Pain Management Following Primary Unilateral TKA
- NCT number
- NCT06112548
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 80 participants, actual
- Lead sponsor
- Damascus University
- Conditions
- Arthritis Knee, Pain, Arthroplasty Complications
- Interventions
- primary unilateral TKA, Bupivacain, ketorolac, epinephrine, Paracetamol, Ketorolac, Tramadol
- First posted
- 2023-11-01
- Last updated
- 2026-03-19
Source ClinicalTrials.gov
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | perception of pain - first assessment | measured 12 hours after surgery. | The severity of knee pain in the short postoperative period. As stated by the patient, on a scale of 0 to 10, 0 resents no pain at all, and 10 is the worst pain the participant can imagine. |
| Primary | perception of pain - second assessment | measured 24 hours after surgery. | The severity of knee pain in the short postoperative period. As stated by the patient, on a scale of 0 to 10, 0 resents no pain at all, and 10 is the worst pain the participant can imagine. |
| Primary | perception of pain - third assessment | measured 48 hours after surgery. | The severity of knee pain in the short postoperative period. As stated by the patient, on a scale of 0 to 10, 0 resents no pain at all, and 10 is the worst pain the participant can imagine. |
| Primary | functional status - first assessment | first measurement four weeks after surgery. | a "Knee Score" section (7 items) and a "Functional Score" section (3 items). Both sections are scored from 0 to 100 with lower scores being indicative of worse knee conditions and higher scores being indicative of better knee conditions. here, the investigator assesses the function section. |
| Primary | magnitude of disabling pain according to KSS - first assessment | first measurement four weeks after surgery. | a "Knee Score" section (7 items) and a "Functional Score" section (3 items). Both sections are scored from 0 to 100, with lower scores being indicative of worse knee conditions and higher scores being indicative of better knee conditions. Here the investigator assesses the pain section. |
| Primary | magnitude of disabling pain according to KSS - second assessment | first measurement six months after surgery. | a "Knee Score" section (7 items) and a "Functional Score" section (3 items). Both sections are scored from 0 to 100, with lower scores being indicative of worse knee conditions and higher scores being indicative of better knee conditions. Here the investigator assesses the pain section. |
| Primary | functional status - second assessment | second measurement six months after surgery. | a "Knee Score" section (7 items) and a "Functional Score" section (3 items). Both sections are scored from 0 to 100 with lower scores being indicative of worse knee conditions and higher scores being indicative of better knee conditions. here, the investigator assesses the function section. |
| Primary | estimated total blood loss | measured once 48 hours after surgery. | the total amount of lost blood in the perioperative period and will be calculated using the Gross formula which is estimated by hitting the patients' blood volume by the difference between pre and post-operative hematocrit value divided by the initial hematocrit value |
| Secondary | perioperative complications | if happened within 6 months of surgery | complications such as Venous thromboembolism VTE, infection, drug side effects ETC |
| Secondary | opioids consumption - frequency | measured once 48 hours after surgery. | the amount of consumed opioids measured by times of application in the close postoperative period |
1 to 10 of 11Source ClinicalTrials.gov
See all 11 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers13
The papers the trial lists on ClinicalTrials.gov.
Grants0
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.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT06112548
GET https://conductscience.org/api/trials/v1/NCT06112548/registered