NCT03795766

Brief Summary

In this cross-section study, all patients in the gynecologic ward of Peking Union Medical College Hospital will accepted a survey about the prevalence and severity of nausea and vomiting according to visual analogue scale and WHO classification. Epidemiological, surgical, anaesthetic characteristics and post-operative treatment are considered as predictors for the post-operative nausea and vomiting. The primary objective is the incidence of nausea and vomiting. The secondary objective is the possible predictors of nausea and vomiting.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2019

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2019

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

January 3, 2019

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 8, 2019

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2020

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2021

Completed
Last Updated

January 8, 2019

Status Verified

January 1, 2019

Enrollment Period

1 year

First QC Date

January 3, 2019

Last Update Submit

January 4, 2019

Conditions

Postoperative Nausea and VomitingGynecologic Surgery

Outcome Measures

Primary Outcomes (1)

  • Incidence of post-operative nausea and vomiting

    Incidence of post-operative nausea and vomiting

    72 hours post-operative

Secondary Outcomes (2)

  • Severity of post-operative nausea and vomiting by visual analogue scale

    72 hours post-operative

  • Severity of post-operative nausea and vomiting by World Health Organization classification

    72 hours post-operative

Interventions

Surgeries for gynecologic diseasePROCEDURE

All patients accept surgeries for gynecologic disease.

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients accept elective surgeries for gynecologic disease with good performance status.

You may qualify if:

  • Aged 18 years or older
  • Elective surgeries for gynecologic disease
  • Good performance status
  • Signed an approved informed consents
  • Post-operative stay 72 hours or longer

You may not qualify if:

  • Emergency surgeries

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Lei Li

Beijing, Beijing Municipality, 100730, China

RECRUITING

MeSH Terms

Conditions

Postoperative Nausea and Vomiting

Interventions

Surgical Procedures, Operative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsNauseaSigns and Symptoms, DigestiveSigns and SymptomsVomiting

Study Officials

  • Lei Li, M.D.

    Peking Union Medical College Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Lei Li

CONTACT

+8613911988831lileigh@163.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

January 3, 2019

First Posted

January 8, 2019

Study Start

January 1, 2019

Primary Completion

January 1, 2020

Study Completion

January 1, 2021

Last Updated

January 8, 2019

Record last verified: 2019-01

Locations

CN(1)