Clinical trial

A Randomized Control Trial of Combined Vaginal Misoprostol and Perivascular Vasopressin During Robotic Myomectomy

Name
2017-03-09
Description
Injection of Vasopressin into the uterine tissue surrounding fibroids constricts blood vessels, and has been found to be beneficial by decreasing blood flow to fibroids, and thereby resulting in less bleeding with removal. Additionally, Misoprostol has been looked at as an additional method to decrease operative blood loss given its ability to increase uterine muscle tone, which therefore constricts the amount of blood flow to the uterus.
Trial arms
Trial start
2017-04-26
Estimated PCD
2019-06-30
Trial end
2019-06-30
Status
Completed
Phase
Early phase I
Treatment
Standard
20 units diluted in 100mL of Normal Saline injected laparoscopic needle
Arms:
Standard-Vaginal Misoprostol
Other names:
Perivascular vasopresssin
Standard-vaginal misoprostol
20 units diluted in 100mL of Normal Saline injected laparoscopic needle and misoprostol 400 mcg
Arms:
Standard, Standard-Vaginal Misoprostol
Other names:
perivascular vasopresssin-vaginal misprostol
Size
74
Primary endpoint
Hemoglobin Levels Difference Between Pre and Post Surgery.
1 hour
Eligibility criteria
Inclusion Criteria: * Reproductive aged women between in ages of 18 to 55 undergoing robotic assisted laparoscopic myomectomy. Exclusion Criteria: 1. History of adverse reaction or allergy to Vasopressin. 2. History of adverse reaction or allergy to Misoprostol. 3. Medical contraindication to use of Vasopressin or Misoprostol 4. Suspicion of possible reproductive cancer with contraindication of morcellation of uterine tissue. 5. Significant medical condition or laboratory result that in the opinion of the Investigator indicate an increased vulnerability to study subject which exposes the subject to an unreasonable risk as a result of participating. 6. Any clinically significant even or condition uncovered during the surgery, such as excessive bleeding or decompensation, that might render the subject medically unstable to continue the study or complicate the subject's intraoperative or postoperative course. 7. Pregnant women
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 74, 'type': 'ACTUAL'}}
Updated at
2024-01-09

1 organization

2 products

3 indications

Product
Standard
Indication
Leiomyoma
Indication
Laparoscopy