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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03364062
Other study ID # GCS-CISR
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 26, 2017
Last updated December 4, 2017
Start date February 10, 2018
Est. completion date December 10, 2019

Study information

Verified date November 2017
Source Peking University People's Hospital
Contact Yichong Zhang, MD
Phone 15210802766
Email 875274428@qq.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To clarify the downward trend of blood pressure affected by bone cement implantation during shoulder replacement operations.


Description:

A total of 350 cases of proximal humeral fracture are planned to be recruited and receive semi-shoulder replacement in Department of Orthopedics and Trauma,Peking University People's Hospital.The blood pressure data are collected from patients' anesthesia records. Both the systolic and diastolic blood pressure are recorded at four time spots during operation: the time before using of bone cement (time period A), 0-5 min after using cement (time period B), 5-10 min after using cement (time period C) and 10-15min after using cement (time period D). The data of blood pressure are collected according to anesthesia records.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 350
Est. completion date December 10, 2019
Est. primary completion date December 10, 2019
Accepts healthy volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

•patients with three or four part of proximal humeral fracture receiving cemented shoulder replacement

Exclusion Criteria:

- pathologic fracture

- severe hypertension or hypotension

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
cemented shoulder replacement
proximal humeral fracture receiving hemi-shoulder replacement with cement when inserting the stem

Locations

Country Name City State
n/a

Sponsors (4)

Lead Sponsor Collaborator
Peking University People's Hospital Dalian Medical University, First Affiliated Hospital of Harbin Medical University, Taoyuan General Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline Systolic Blood Pressure the systolic blood pressure after insert the cemented stem Change from Baseline Systolic Blood Pressure at 15 mins
Secondary Change from Baseline Diastolic Blood Pressure the diastolic blood pressure after insert the cemented stem Change from Baseline Diastolic Blood Pressure at 15 mins
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