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Trial · NCT07884994

HUGO-SLEEVE: Evaluating the Feasibility of Robotic Sleeve Gastrectomy With a New Platform

NCT07884994, Not applicable, Recruiting, Universitätsklinikum Hamburg-Eppendorf

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. HUGO-SLEEVE: Evaluating the Feasibility of Robotic Sleeve Gastrectomy With a New Platform. Trials, record NCT07884994. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07884994

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
HUGO-SLEEVE: Evaluating the Feasibility of Robotic Sleeve Gastrectomy With a New Platform
NCT number
NCT07884994
Status
Recruiting
Phases
Not applicable
Enrollment
50 participants, estimated
Lead sponsor
Universitätsklinikum Hamburg-Eppendorf
Conditions
Obesity (BMI > 35), Obesity (BMI > 35) and Diabetes Mellitus, Obesity (BMI > 35) and Dyslipemia, Obesity (BMI > 35) and High Blood Pressure
Interventions
Sleeve Gastrectomy using Hugo RAS platform
First posted
2026-10-21
Last updated
2026-10-21

Source ClinicalTrials.gov

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primary
Proportion of robotic sleeve gastrectomy procedures successfully completed using the Hugo™ Robotic-Assisted Surgery (RAS) system including LigaSure™ RAS without intraoperative conversion to conventional laparoscopy or open surgery.
From beginning to the end of the Procedure
SecondaryPort Placement TimeDuring surgeryTime interval from skin incision to initiation of robotic system setup and docking
SecondaryDocking TimeDuring surgeryTime interval from completion of port placement to console readiness
SecondaryConsole TimeDuring surgeryDuration of active use of the Hugo™ robotic surgical console
SecondaryTotal Operative TimeDuring surgeryTime interval from skin incision to skin closure (skin-to-skin time)
SecondaryIntraoperative ComplicationsDuring surgeryOccurrence of intraoperative complications, such as bleeding or stapling-related issues
SecondaryPostoperative Complication RateWithin 30 days after surgeryOccurrence of postoperative complications
SecondaryLength of Hospital StayAssessed up to postoperative day 30Duration of postoperative hospital stay
SecondaryReadmission RateWithin 6 months after surgeryHospital readmission after sleeve gastrectomy
SecondaryReoperation RateWithin 6 months after surgeryRequirement for reoperation following sleeve gastrectomy

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07884994

GET https://conductscience.org/api/trials/v1/NCT07884994/registered