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Evaluating the Novel Veress Plus Needle

NCT05613959 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 18

Last updated 2022-11-14

No results posted yet for this study

Summary

18 participants (novices, intermediates and experts) performed in total 248 insertions in a systematic way on Thiel embalmed bodies with wide and small bore versions of the conventional VNc (conventional Veress Needle) and the VN+(The Veress Needle plus). Insertion depth was measured by recording the graduations on the needle under direct laparoscopic vision.

Conditions

  • Pneumoperitoneum

Interventions

DEVICE

Veress +

The Veress+ safety mechanism was used

DEVICE

Conventional Veress

The Conventional Veress Needle was used

Sponsors & Collaborators

  • Prof Jean Calleja-Agius

    lead OTHER

Principal Investigators

  • Jean Calleja Agius, MD PhD · University of Malta

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-01-01
Primary Completion
2021-09-26
Completion
2021-09-26

Countries

  • Malta

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05613959 on ClinicalTrials.gov