Blood Loss, Surgical Clinical Trial
Official title:
Intraoperative Repolarisation - Etiology and Relevance for the Decision Making by Anesthesiologists in the Management of Volume Substitution and Transfusion
NCT number | NCT02441751 |
Other study ID # | EK110032015 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | May 2015 |
Est. completion date | December 31, 2023 |
QT interval changes is measured during all phases of the operation. The protocol is focusing at intraoperative bleeding events and is also observing QT interval changes during anesthetic and operative procedures.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | December 31, 2023 |
Est. primary completion date | June 30, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - American Society of Anesthesiologists physical status classification 2 - 3 - patients after consent Exclusion Criteria: - Children, - pregnant women, - patients not able to consent |
Country | Name | City | State |
---|---|---|---|
Germany | Dept. of Anesthesia and Intensive Care, University Hospital, Technische Universität Dresden | Dresden |
Lead Sponsor | Collaborator |
---|---|
Technische Universität Dresden |
Germany,
Straus SM, Kors JA, De Bruin ML, van der Hooft CS, Hofman A, Heeringa J, Deckers JW, Kingma JH, Sturkenboom MC, Stricker BH, Witteman JC. Prolonged QTc interval and risk of sudden cardiac death in a population of older adults. J Am Coll Cardiol. 2006 Jan 17;47(2):362-7. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change in QT-time | during operation | ||
Secondary | postoperative incidents/disturbance rhythm of the heart | association to intraoperative repolarisation-disturbance / QT-prolongation | 2 days | |
Secondary | survival | association to intraoperative repolarisation-disturbance / QT-prolongation | 1 year |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04114253 -
QStat in Liver Transplant
|
||
Recruiting |
NCT05077124 -
Safe and Timely Antithrombotic Removal (STAR) Registry
|
||
Active, not recruiting |
NCT03651154 -
Hypovolemic Phlebotomy to Reduce Blood Transfusions in Major Hepatic Resections
|
N/A | |
Recruiting |
NCT04519593 -
ABSOLUTELY: A Temporary Uterine Blood Supply Occlusion for Laparoscopic Myomectomy in Patients With UTErine LeiomYoma
|
N/A | |
Completed |
NCT02043132 -
Tranexamic Acid in Reverse Total Shoulder Arthroplasty
|
Phase 2/Phase 3 | |
Withdrawn |
NCT00861367 -
Prospective Double-blind Study for the Use of Aspirin During Transurethral Surgery of the Bladder or the Prostate
|
N/A | |
Terminated |
NCT03246919 -
Ideal Time of Oxytocin Infusion During Cesarean Section
|
Phase 4 | |
Completed |
NCT04443920 -
Tranexamic Acid for Total Knee Arthroscopy
|
Phase 4 | |
Withdrawn |
NCT04933253 -
Mediastinal Temperature and Post-operative Bleeding
|
N/A | |
Recruiting |
NCT02938962 -
Intravenous vs. Topical Tranexamic Acid in Revision THA (VITALITY-X)
|
Phase 4 | |
Recruiting |
NCT02130752 -
Ultrasonic Scalpel vs. Monopolar Electrocautery for D2 Distal Gastric Carcinoma Surgery
|
N/A | |
Recruiting |
NCT05164809 -
Effect of Electrosurgery on Blood Loss and Intraoperative Transfusions in Musculoskeletal Tumor Surgery
|
||
Not yet recruiting |
NCT04574128 -
Retransfusion or Not of Cardiotomy Blood
|
N/A | |
Completed |
NCT02911831 -
IV Tranexamic Acid Prior to Hysterectomy
|
Early Phase 1 | |
Completed |
NCT02740374 -
Evaluation of Thromboelastometry (ROTEM) During Spinal Surgery
|
N/A | |
Enrolling by invitation |
NCT05474027 -
Reducing Hypotensive Anesthesia Use With TXA During Orthognathic Surgery
|
Phase 4 | |
Completed |
NCT05391607 -
Comparison Between Hyperoncotic and Isooncotic Albumin to Support Blood Loss Replacement
|
Phase 4 | |
Completed |
NCT03152461 -
Evaluation of the Clinical Performance of the Quantra System With the Quantra Surgical Cartridge
|
||
Completed |
NCT01053169 -
Observational Study of Prophylaxis and Treatment of Acute Perioperative Bleeding With Beriplex® P/N (Probe Study)
|
N/A | |
Completed |
NCT00656396 -
Point of Care Coagulation Testing in Patients Undergoing Major Surgery
|
Phase 3 |