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NCT05624463Completed

Effect of Modified Endotracheal Intubation Protocol Combined With Early Oral Intake on Postoperative Recovery Quality in Thyroid and Parathyroid Surgery

Effect of Modified Endotracheal Intubation Protocol Combined With Early Oral Intake on Postoperative Recovery Quality in Thyroid and Parathyroid Surgery at a Tertiary Hospital in China: A 2x2 Factorial Randomized Controlled Trial Protocol

Source: ClinicalTrials.gov · Last updated 1 Apr 2024

Brief summary (registry, in English)

The purpose of this study is to assess the effect of modified endotracheal intubation procedure combined with early oral intake on postoperative recovery quality of patients, so as to further optimize the ERAS(enhanced recovery after surgery) program for thyroid or parathyroid surgery.

Status (registry)
Completed
Study type
Interventional
Enrollment
200 (actual)
First submitted
13 Nov 2022
Start date
1 Apr 2023
Primary completion date
6 Feb 2024
Lead sponsor
Peking Union Medical College Hospital
NCT number
NCT05624463

What you commit to

  • Study type: Interventional
  • Participants enrolled: 200
  • From 1 Apr 2023 to the primary completion date, 6 Feb 2024
  • 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

  • Patients or family members cannot understand the conditions and objectives of this study
  • Exclusion criteria of Quality of Recovery-15\* (\*Quality of Recovery-15 exclusion criteria: 1. Unable to understand words and language; 2. Difficult to cooperate due to mental disorders; 3. History of alcohol or drug abuse; 4. Any serious pre-existing medical condition that can limit the objective evaluation after surgery; 5. Any life-threatening complications; 6. Emergency surgery)

Other

  • Preoperative patients with acute pharyngitis, hoarseness, cough, dysphagia, and high risk of aspiration
  • The surgeons or anesthesiologists point out that the patient is not suitable for early postoperative drinking (such as considering the injury of recurrent laryngeal nerve or lymphatic vessels during the operation)
  • Patients who cannot be intubated under visual laryngoscope(such as difficult airway, loose incisors and so on)

Who the study is looking for

  • Age ≥ 18
  • American Society of Anesthesiologists (ASA) physical status classification I-II
  • Body mass index 18.5-29.9kg/m2
  • First operation on operation day

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Peking Union Medical College Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

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