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Sedation Versus No Sedation for Detection Rates of Precancerous Lesions and Cancer

Sedation Versus No Sedation for Diagnostic Esophagogastroduodenoscopies and Detection Rates of Precancerous Lesions and Cancer: a Case-control Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04069975
Enrollment
200000
Registered
2019-08-28
Start date
2019-06-02
Completion date
2020-06-30
Last updated
2019-08-30

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

Conditions

Early Detection of Cancer

Keywords

Early Detection of cancer, Gastrointestinal Neoplasms, Endoscopy, Gastrointestinal

Brief summary

The influence of sedation on the endoscopic detection rate of the precancerous lesions and cancer of upper digestive system has not been assessed. In the daily medical routine of China, patients have the right to choose the sedation style according to his or her own situation, whose detailed endoscopic data of patients are recorded in the endoscopy quality control system. The aim of this research is to detect whether the use of sedation can help improve detection rate of precancerous lesions and cancer of upper digestive system.

Detailed description

The influence of sedation on the endoscopic detection rate of the precancerous lesions and cancer of upper digestive system has not been assessed. In the daily medical routine of China, patients have the right to choose the sedation style according to his or her own situation, whose detailed endoscopic data of patients are recorded in the endoscopy quality control system. The aim of this research is to detect whether the use of sedation can help improve detection rate of precancerous lesions and cancer of upper digestive system.

Interventions

OTHERSedation

The group of patients who did endoscopies with or without sedation. (This is a choice of themselves)

Sponsors

Weihai Municipal Hospital
CollaboratorOTHER
Binzhou Medical University
CollaboratorOTHER
Qilu Hospital of Shandong University (Qingdao)
CollaboratorOTHER
Shandong University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients aged more than 18 years with or without GI symptoms attending for endoscopy from 2012 to 2019.

Exclusion criteria

* Patients unable to cooperated the endoscopy or unable to complete it. People with endoscopy contraindications are naturally excluded.

Design outcomes

Primary

MeasureTime frameDescription
Detection rate of precancerous lesions and cancer of upper digestive system improvement2020Detection rate of precancerous lesions and cancer of upper digestive system improvement

Countries

China

Contacts

Primary ContactYanqing LI, Doctor
liyanqing@sdu.edu.cn13573106261

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026