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Influence of Analgesia and Neuromuscular Block on Abdominal Distension and Operating Conditions Laparoscopic Operations

NCT03605628 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2022-08-17

No results posted yet for this study

Summary

Neuromuscular block improves operation conditions during laparoscopic surgery. In this study, a new measurement tool is assessed: the degree of abdominal distension during the time course of the neuromuscular block is measured and compared with a standardized score (surgical rating score).

Conditions

  • Neuromuscular Blockade

Interventions

OTHER

measuring tape

measurement of change in abdominal wall length \[cm\] during neuromuscular block with a measuring tape.

OTHER

neuromuscular block

Measurement of the time course of the neuromuscular block: neuromuscular transmission is measured by assessment of the post tetanic count and the train of four ratio using acceleromyography (TOF Watch SX™, Essex Pharma GmbH, Munich, Germany) at the right adductor pollicis muscle with transcutaneous Ag/AgCl electrodes (electrocardiogram electrodes; Ambu Inc., MD 21060 USA);

OTHER

Surgical rating score

assessment of operating conditions by means of a standardized score: surgical rating score: 1. extremely poor conditions 2. poor conditions 3. acceptable conditions 4. good conditions 5. optimal conditions

Sponsors & Collaborators

  • Kreiskrankenhaus Dormagen

    lead OTHER

Principal Investigators

  • Stefan Soltesz, MD · Kreiskrankenhaus Dormagen

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-01
Primary Completion
2019-06-30
Completion
2019-06-30

Countries

  • Germany

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 NCT03605628 on ClinicalTrials.gov