Recruiting

Desmopressin

Sponsor:

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Code:

NCT07179991

Conditions

Intraoperative Bleeding

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Desmopressin after protamine reversal

Study Details

Brief summary:

Cardiopulmonary bypass (CPB) is a process that uses a pump that temporarily takes over the function of the heart and lungs during cardiac surgery to maintain blood circulation and oxygenation. Using CPB during cardiac surgery can result in complications with blood clotting. Blood clotting is achieved when molecules in the blood, called platelets, are able to form together with the help of other clotting factors to form a clot. A drug called desmopressin (DDAVP) is used to help blood clot properly by increasing the amount of clotting factors in the blood. Several studies have shown that desmopressin has the ability to reduce the amount of blood transfusions needed for cardiac surgery patients in the postoperative period. At LHSC desmopressin is frequently requested by Cardiac Surgeons and Anesthesiologists to stop bleeding and promote blood clotting where required. A test called TEG6s platelet mapping is a blood test used to help manage the use of blood products by being able to provide information on platelet function and blood clotting activity. At the moment, there is a lack of information regarding the use of TEG6s platelet mapping to analyze the effect of desmopressin on blood clotting in cardiac surgery patients after CPB. The purpose of this study is to investigate the dose-related effects of desmopressin on platelet function in patients undergoing cardiac surgery with CPB. By using TEG6s platelet mapping, this study aims to observe dynamic changes in platelet function following desmopressin administration at various time points in the perioperative and postoperative periods.

Conditions

Intraoperative Bleeding

Study ID

NCT07179991

Start date

Aug 1, 2026

Status verified date

Sep, 2026

Completion date

Dec 31, 2028

Anticipated

Primary completion date

Dec 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Age 18 years and above
2. Undergoing elective cardiac surgery with cardiopulmonary bypass
3. Able to provide informed consent

Exclusion Criteria:

1. Hyponatremia
2. Allergy to desmopressin or its components
3. History of coronary artery disease with thrombosis
4. Recent history of thromboembolic events (Stroke/TIA/DVTs)
5. Severe Renal Impairment Creatinine Clearance<30 ml/min
6. Inability to communicate in the English language

Study Design

Enrollment

100 participants

Anticipated

Interventions and Outcome Measures

Arms

Desmopressin after protamine reversal

Desmopressin will be given to participants at a dose of 0.3mcg/kg after protamine reversal at the end of cardiopulmonary bypass (CPB).

Interventions

Desmopressin after protamine reversal

Desmopressin will be given to participants at a dose of 0.3mcg/kg after protamine reversal at the end of cardiopulmonary bypass (CPB).

Platelet function will be assessed by TEG (Thromboelastography) platelet mapping at the following points:

1. T1 TEG6s: after arterial line insertion before skin incision.
2. T2 TEG6s: after protamine (baseline function after CPB)
3. T3 TEG6s: 30 minutes after desmopressin
4. T4 TEG6s: 6 hours after (intensive care unit) ICU admission
5. T5 TEG6s: 24hours after ICU admission

Primary outcome measure

  • Change in platelet function due to desmopressin administration after cardiopulmonary bypass [ Time Frame: After arterial line insertion - 24 hours after admission to the intensive care unit ]

Central Contacts and Locations

Central contacts

Locations

London Health Sciences Centre

Recruiting

London, Ontario, Canada, N6A 5A5

Contacts

More Information

Sponsor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Last update posted

Sep 21, 2026

Last verified

Sep, 2026

Keywords

  • Desmopressin
  • Cardiopulmonary bypass

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-24. This information was provided to ClinicalTrials.gov by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's on 2026-09-21. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.