NCT05252234

Brief Summary

Estimating and recording the rate of occurrence of pulmonary and cardiovascular complications during the perioperative period in patients with past covid infection

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
180

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Apr 2022

Shorter than P25 for all trials

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

First Submitted

Initial submission to the registry

February 19, 2022

Completed
4 days until next milestone

First Posted

Study publicly available on registry

February 23, 2022

Completed
1 month until next milestone

Study Start

First participant enrolled

April 1, 2022

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2022

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2022

Completed
Last Updated

March 15, 2022

Status Verified

March 1, 2022

Enrollment Period

3 months

First QC Date

February 19, 2022

Last Update Submit

March 12, 2022

Conditions

Intraoperative HypertensionPain ThresholdPostoperative PainPostoperative Hypoxemia

Keywords

SARS-Cov-2Anesthesia

Outcome Measures

Primary Outcomes (1)

  • Rate of occurrence of pulmonary and cardiovascular complications

    Measure all vital data and postoperative status

    24 hours

Study Arms (1)

Group 1

Patients undergoing elective surgeries with past history of COVID-19 infection during the past six months

Other: Observation of hemodynamic status and post operative pain

Interventions

Observation of hemodynamic status and post operative painOTHER

No intervention

Group 1

Eligibility Criteria

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

Above 18 years undergoing surgery with past history of covid-19

You may qualify if:

  • all patients above 18 years with past history of covid-19 during past 6 months undergoing surgery

You may not qualify if:

  • hemodynamically unstable Patients requiring oxygen therapy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of medicine, Ain Shams University

Cairo, Egypt

Location

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Officials

  • Fathy Tash, MD

    Ain Shams University

    STUDY CHAIR

Central Study Contacts

Amr M Hilal Abdou, MD

CONTACT

01001479037Amr_hilal@med.asu.edu.eg

Study Design

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

Study Record Dates

First Submitted

February 19, 2022

First Posted

February 23, 2022

Study Start

April 1, 2022

Primary Completion

June 30, 2022

Study Completion

September 30, 2022

Last Updated

March 15, 2022

Record last verified: 2022-03

Data Sharing

IPD Sharing
Will share
Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR
Time Frame
6 months

Locations

EG(1)