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Modified chest compression for the prevention and treatment of propofol-induced respiratory depression in patients with painless gastroscopy

Modified chest compression for the prevention and treatment of propofol-induced respiratory depression in patients with painless gastroscopy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013174
Enrollment
Unknown
Registered
2017-10-30
Start date
2017-11-01
Completion date
Unknown
Last updated
2021-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

respiratory suppression in painless gastrocopy

Interventions

Preventive control group:Nonintervention
Preventive chest compression group:Modified chest compression (right chest compression parallel to the sternum angle)14, the compression range was 2 to 3 cm, and the frequency was 100-120 times/min, a
Therapeutic control group:Nonintervention
Therapeutic chest compression group:Modified chest compression (right chest compression parallel to the sternum angle)14, the compression range was 2 to 3 cm, and the frequency was 100-120 times/min,

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients age 18 to 65 years who were American Society of Anesthesiologists (ASA) class I to ? and were scheduled for elective painless gastroscopy were included in the study. All patients signed an informed written consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria were: (1) refused to participate in the study or were participating in another clinical trial; (2) complicated with serious dysfunction of vital organ function: including serious dysfunction of heart, lung, liver and kidney, (3) severe coagulation dysfunction, (4) thoracic deformity and rib fracture, chest and abdominal trauma, chest and abdominal surgery within 6 months, (5) pregnancy, (6) basic blood oxygen saturation lower than 95%, (7) a history of neurological, mental illness or other reasons can not cooperate with the visitor, (8) serious complications occur during examination, such as massive bleeding and organ damage, (9) loss of visit or failure to follow the visitors as required.

Design outcomes

Primary

MeasureTime frame
Incidence of hypoxemia(SPO2<95%);The lowest value of SpO2;

Secondary

MeasureTime frame
The minimum of SpO2<95%;The frequency of SpO2<95%;Incidence of severe hypoxemia (SpO2<85%);The frequency of SpO2<85%;Time from induction to the onset of hypoxemia;Snoring after anesthesia;Incidence and duration of apnea;Improvement rate after mandibular support and head reclining;Gastroscope withdrawal rate;Total dosage of propofol;Total time of inspection;Anesthesia recovery time;Postoperative adverse reactions;Satisfaction scores of endoscopists and patients;

Countries

China

Contacts

Public ContactXiaoyun Li

The Third Affiliated Hospital of Sun Yat-Sen University

13113361686@126.com+86 13113361686

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026