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The Effect of Tranexamic Acid (TXA) on Visualization During Shoulder Arthroscopy

Rothman Institute Orthopaedics logo

Rothman Institute Orthopaedics

Status and phase

Unknown
Phase 3

Conditions

Operative Bleeding
Postoperative Pain
Shoulder Arthroscopy

Treatments

Drug: Tranexamic acid

Study type

Interventional

Funder types

Other

Identifiers

NCT04610164
SNAM18d.610

Details and patient eligibility

About

Tranexamic acid has seen an increase in use over the past decade in hip and knee arthroplasty as well as spine surgery with more recent use seen in total shoulder arthroplasty (TSA). The mechanism of action of TXA is as a lysine analogue that competitively inhibits the conversion of plasminogen to plasmin thus resulting in its antifibrinolytic activity. Investigators have showed that compared with placebo TXA had a statistically significant effect on blood and postoperative hemoglobin levels in TSA. To date there are no studies investigating the effect of TXA in arthroscopy of any kind or studies examining the ability of TXA to aid in surgeon visualization in arthroscopic procedures. The investigators of this study will use change in pump pressure as a surrogate objective measure for surgeon visualization. The hypothesis is that participants who receive TXA will have a lower change in pump pressure compared to participants who do not receive TXA.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • participants aged 18-80
  • participants with an ASA (American Society of Anesthesiologists) score 1-3
  • participants with a surgical indication of full thickness small to massive rotator cuff tear.

Exclusion criteria

  • pregnant females,
  • participants with a known allergy to tranexamic acid,
  • participants with active thromboembolic disease,
  • participants with seizure disorder,
  • participants with prior cerebrovascular accident (CVA),
  • history of cardiac stents or past history of thromboembolic disease,
  • presence of full-thickness subscapularis tear (>50%),
  • participants with irreparable rotator cuff tears.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

200 participants in 2 patient groups

Group 1: TXA group
Experimental group
Description:
Patient will receive 1 gram intravenous TXA prior to surgery
Treatment:
Drug: Tranexamic acid
Group 2: Control Group
No Intervention group
Description:
Patient will not receive TXA prior to surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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