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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03026920
Other study ID # HZY2015
Secondary ID
Status Recruiting
Phase N/A
First received January 18, 2017
Last updated December 13, 2017
Start date June 2016
Est. completion date June 2018

Study information

Verified date January 2017
Source Hebei Medical University Third Hospital
Contact Zhiyong Hou, M.D
Phone +8618533112800
Email houzhiyong1234@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It was reported that satisfactory postoperative outcome was difficult to obtain for the pelvic or acetabular fracture in old people. The less invasive surgical method was conducted in this study. Then, the clinical results were compared with the patients treated using traditional methods to assess the less invasive method.


Description:

Pelvic or acetabular fractures were caused by high energy trauma, which may lead to poor prognosis for the old. The patients over 60 years were included in this study. The surgical procedure was conducted in two weeks. The less invasive methods involved Stoppa approach and novel plate. The data including surgical time, blood loss and results of follow-up were recorded. The clinical results were compared with the patients treated using traditional methods. Thus, the clinical outcome of Pelvic or acetabular fractures in old man was assessed.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date June 2018
Est. primary completion date December 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

Over 60 years old Fracture involving pelvis or acetabulum Operation was conducted within 14 days Sign the consent form

Exclusion Criteria:

Presented with a pathologic acetabular fracture Refused to participate Follow-up insufficient 12 months

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
less invasive method
The less invasive surgical method was conducted in this study. Then, the clinical results were compared with the patients treated using traditional methods to assess the less invasive method.

Locations

Country Name City State
China Hebei Medical University Third Hospital Shijiazhuang Hebei

Sponsors (1)

Lead Sponsor Collaborator
Hebei Medical University Third Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary fracture union time how long the fracture line disappeared postoperatively in radiograph 4 months
Secondary complication wound infection, iatrogenic injury of vessels and nerves, nonunion 12 months
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