Postoperative Complications Clinical Trial
Official title:
Surgeon Perception of Gastric Decompression at Time of Gynecologic Laparoscopy, a Randomized Control Trial
The goal of this clinical trial is to test whether it is necessary to decompress the stomach during gynecologic laparoscopy. The main questions it aims to answer are: - Is there appropriate visualization during surgery without stomach decompression? - Can the surgeon tell the stomach is decompressed? - Is the stomach at risk for injury during surgery? - How is the patient's postoperative experience affected? Participants will undergo their planned surgery as usual and will be asked to complete log about their recovery for the first week after surgery. Researchers will compare patients who have their stomach decompressed during surgery to those who do not undergo stomach decompression to see if it is necessary.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | January 2025 |
Est. primary completion date | November 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Undergoing gynecologic laparoscopy for the following indications: hysterectomy, adnexal surgery, benign and malignant tumors or disease, diagnostic purposes, lysis of adhesions, and pelvic pain. - Surgery being performed by gynecologic surgeon with or without minimally invasive gynecologist certification, gynecologic oncologists, urogynecologists, and reproductive endocrinologists. Exclusion Criteria: - Entry sites other than umbilical - Planned or high suspicion for bowel surgery - Anticipated surgical time >4 hours - Known diagnosis of gastric reflux disease or peptic ulcer disease - Prior history of gastric or esophageal surgery excluding endoscopy - Day of surgery emesis events - Difficult intubation determined by anesthesia - Intrauterine pregnancy - Chronic lung disease - Individuals with smoking history. - Individuals who do not speak English due to limitations in ability to reliably obtain informed consent in their primary language. |
Country | Name | City | State |
---|---|---|---|
United States | 259 E Erie - Northwestern | Chicago | Illinois |
United States | Prentice Women'S Hospital | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Northwestern University |
United States,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Adequate gastric decompression | The primary endpoint is the percentage of cases rated as adequate decompression by the surgeon. | At time of surgery | |
Primary | Gastric injury | The primary safety endpoint is the estimated negligible rate of gastric injury. | Up to six weeks post-operatively | |
Secondary | Presence of gastric decompression tube | Accurate determination of presence of orogastric or nasogastric tube via intraoperative survey | At time of surgery | |
Secondary | Gastric injury risk assessment | Percentage of cases in which the surgeon believes the stomach was at risk for injury during umbilical entry | At time of surgery | |
Secondary | Degree of stomach decompression | Perceived degree of stomach decompression, rated qualitatively as "excellent," "good," "fair," or "poor" | At time of surgery | |
Secondary | Entry proximity | Estimated distance between the umbilicus and stomach on abdominal entry | At time of surgery | |
Secondary | Post-operative experience questionnaire | Patients' postoperative experience including rates of nausea and vomiting, nasal, and oropharyngeal discomfort, and time to return of bowel function as measured by a patient reported symptom log | First 7 days after surgery | |
Secondary | Post-operative complications | A secondary safety endpoint is rates of postoperative complications which may be related to gastric decompression including aspiration or pneumonia as measured by electronic medical record chart review post operatively. | Up to six weeks post-operatively |
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