Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06479161 · ClinicalTrials.gov registry record · Phase 2

Effects of Oral Tranexamic Acid Following Total Knee Arthroplasty

A Phase 2 study of Postoperative Pain, sponsored by Matthew Grosso, MD.

Recruiting
Registry status
Phase 2
Development phase
80
Enrollment target
1
Study location

NCT06479161: Recruiting Phase 2 study of Postoperative Pain, sponsored by Matthew Grosso, MD.

NCT06479161 is a Phase 2 study of Postoperative Pain that is actively recruiting participants, run by Matthew Grosso, MD. The registered enrollment target is 80 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (65% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06479161, a Phase 2 study of Postoperative Pain, is actively recruiting participants, sponsored by Matthew Grosso, MD.

RECRUITING
Registry status
Phase 2
Development phase
80 participants
Enrollment target
1
Study location

Study Summary

The primary purpose of this study is to evaluate postoperative pain. Secondary outcomes evaluated in this study will include range of motion (ROM), opioid consumption, and ambulation. Each outcome measure will be evaluated, oral tranexamic acid (TXA) in the experiment arm and placebo in the control arm, after total knee arthroplasty (TKA) at postoperative days 0-3, and weeks 1, 2, 6, and 12.

Primary Outcome

Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain. Higher scores are a worse outcome.

Conditions Studied

Interventions

  • DRUG Tranexamic acid

Study Locations (1)

Connecticut

  • Trinity Health Of New England/CT Joint Replacement Institute - Hartford

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2024-06-10
Est. Completion 2025-03-30
Phase Phase 2
Matthew Grosso, MD

1 total trials

What NCT06479161 shows while recruiting

NCT06479161 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (65% lower).

The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 1 intervention - of which Tranexamic acid is the first listed.

NCT06479161 reports a single indexed study location in Connecticut.

Frequently Asked Questions

What is clinical trial NCT06479161 about?

NCT06479161 is a clinical study titled "Effects of Oral Tranexamic Acid Following Total Knee Arthroplasty". The primary purpose of this study is to evaluate postoperative pain. Secondary outcomes evaluated in this study will include range of motion (ROM), opioid consumption, and ambulation. Each outcome measure will be evaluated, oral tranexamic acid (TXA) in the experiment arm and placebo in the control ...

What is the current status of trial NCT06479161?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 80 participants. The study started on 2024-06-10. Estimated completion is 2025-03-30.

What conditions does trial NCT06479161 study?

This clinical trial studies the following conditions: Postoperative Pain.

What interventions are being tested in trial NCT06479161?

The interventions under investigation include: Tranexamic acid (DRUG).

Who is sponsoring clinical trial NCT06479161?

This trial is sponsored by Matthew Grosso, MD, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06479161 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Postoperative Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06479161's enrollment target sits among peer trials

80 69th of 120 higher than 47 of 120 other Postoperative Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Postoperative Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01243931 · 80 participants · NA

    Optical Coherence Tomography Guided Transepithelial Phototherapeutic Keratectomy

  • NCT01659203 · 80 participants · Phase 1

    Proton or Photon RT for Retroperitoneal Sarcomas

  • NCT01803451 · 80 participants · Early Phase 1

    Glucagon-like Peptide 1, Glucose Metabolism and Gastric Bypass

  • NCT01964859 · 80 participants · Phase 2

    Feasibility Study for Fibroblast Autologous Skin Grafts

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06479161, the US trial registry maintained by the National Library of Medicine. NCT06479161 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.