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Minimally Invasive Surgery: Using Natural Orfices

Natural Orifice Translumenal Endoscopic Surgery (NOTES): Laparoscopic Assisted Trans-Vaginal Appendectomy and Cholecystectomy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00530998
Acronym
NOTES
Enrollment
120
Registered
2007-09-18
Start date
2007-09-30
Completion date
2019-09-30
Last updated
2020-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Appendicitis, Cholelithiasis, Gallstones

Keywords

appendicitis, cholelithiasis, Gallstones

Brief summary

This is an observational study of pain and outcomes from females undergoing transvaginal NOTES removal of their appendix or gallbladder. Female subjects who elect to have a transvaginal NOTES removal of their appendix or gallbladder and agree to be in this study (through signature on the informed consent form) will be followed per standard of care, with additional follow-up for data collection including the following: * Subjects will complete a 7 day pain/temperature log after surgery * Subjects will complete a standardized sexual function questionnaire (Female Sexual Function Index) prior to surgery and 6 months after surgery * Subjects will receive a phone call at 6 months and at 1 year after surgery to capture data related to safety, adverse events, hospitalizations and patient satisfaction Additional data related to pain and outcomes will be collected at baseline/screening and at follow-up as necessary.

Interventions

The appendix will be removed via an incision in the vagina.

The gallbladder will be removed via an incision in the vagina.

Sponsors

University of California, San Diego
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

for transvaginal appendectomy: 1. Females between the ages of 18-75 2. Clinical diagnosis of appendicitis 3. Emergency room evaluation within 36 hours of the onset of pain 4. ASA Classification 1 5. Mentally competent to give informed consent 6. Scheduled to undergo a transvaginal NOTES appendectomy.

Exclusion criteria

for transvaginal appendectomy: 1. Pregnant women (need to have negative icon in ER) 2. Morbidly obese patients (BMI \>35) 3. Patients who are taking immunosuppressive medications or are immunocompromised 4. Patients with evidence of an abdominal abscess or mass 5. Patients who present with a clinical diagnosis of sepsis or peritonitis 6. Patients who have a history of prior transvaginal surgery. Patients with prior laparoscopic surgery will be included. 7. Patients who endorse a history of ectopic pregnancy, pelvic inflammatory disease (PID), or severe endometriosis 8. Patients with diffuse peritonitis on clinical exam 9. Patients on blood thinners or aspirin or abnormal blood coagulation tests Inclusion criteria for transvaginal cholecystectomy: 1. Females between the ages of 18 and 75 2. Diagnosis of gallstone disease which requires cholecystectomy 3. ASA class 1 4. Mentally competent to give informed consent 5. Scheduled to undergo a transvaginal NOTES cholecystectomy

Design outcomes

Primary

MeasureTime frame
To evaluate the safety and efficacy of transvaginal NOTES appendectomies and cholecystectomies (through data collection).1 year

Secondary

MeasureTime frame
To evaluate pain associated with the transvaginal approach (through data collection).1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026