Fact CheckerSign in

NCT06549244Completed

Preoperative Maximum Inspiratory Pressure and Outcomes After Interscalene Block in Obese Patients

A Pilot Study on Inspiratory Dynamics and the Effect of Body Mass Index on Respiratory Outcomes After Temporary Hemi Diaphragmatic Paresis Related to Brachial Plexus Blocks

Source: ClinicalTrials.gov · Last updated 12 Aug 2024

Brief summary (registry, in English)

The study aims to explore if Maximum Inspiratory Pressure can predict postoperative breathlessness in obese patients receiving interscalene blocks for shoulder surgery. The main question is: does baseline Maximum Inspiratory Pressure have any association with postoperative breathlessness after interscalene blocks in class 2 or higher obese patients (BMI\>35). Preoperative and postoperative lung volumes, pressures, breathlessness score and respiratory outcomes will be measured on participants already receiving shoulder surgery with interscalene blocks.

Status (registry)
Completed
Study type
Observational
Enrollment
45 (actual)
First submitted
31 Jul 2024
Start date
1 Jul 2023
Primary completion date
28 Nov 2023
Lead sponsor
University of North Carolina, Chapel Hill
Diseases
Obesity
NCT number
NCT06549244

What you commit to

  • Study type: Observational
  • Participants enrolled: 45
  • From 1 Jul 2023 to the primary completion date, 28 Nov 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • those with significant neuromuscular disease, tracheo-bronchial structural abnormalities, severe respiratory or severe cardiovascular comorbidity;

Age

  • Less than 18 years of age;

Other

  • currently pregnant;
  • currently incarcerated;
  • those undergoing intra-abdominal or intrathoracic surgeries due to the potential to independently effect breathing

Who the study is looking for

  • Adults \>18 years of age receiving shoulder surgery with preoperative interscalene block and general anesthesia;
  • Speak English;
    • Group 3
  • Adults \>18 years of age receiving cystoscopy or lower extremity procedures receiving general endotracheal anesthesia

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of North Carolina
Coordinator of this site? Confirm its status
Chapel HillUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.