Whether Patients With Achilles Tendon Tears Have Different Lipid Levels Than Healthy People: a Retrospective Study

July 4, 2021 updated by: Peking University Third Hospital
To explore the difference of blood lipid levels between patients with Achilles tendon rupture and healthy people without Achilles tendon rupture, and to provide clues for further exploration of its mechanism.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Data were collected from 287 patients with Achilles tendon rupture repaired by Yang Yuping, deputy chief physician of the Institute of Sports Medicine of Peking University Third Hospital from January 2017 to December 2017. A total of 10,375 subjects who underwent physical examination in the Physical Examination Center of Peking University Third Hospital during the same period were selected as the control group, and 9,193 subjects were selected as the control group after excluding patients without blood lipid test results, professional athletes, hypertension and diabetes patients. The general data, blood glucose, blood lipid, blood uric acid, smoking and alcohol consumption of the subjects were collected through the hospital information system. The blood glucose, blood lipid, uric acid and other data of the control group and the Achilles tendon rupture group were detected, and it was concluded that the blood lipid level of the patients with Achilles tendon rupture group was higher than that of the control group.

Study Type

Observational

Enrollment (Actual)

10662

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • China
    • Beijing
      • Beijing, Beijing, China, 100191
        • Peking Univerisity Third Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Yang Yuping, Deputy Chief Physician of the Institute of Sports Medicine of Peking University Third Hospital from January 2017 to December 2017 in Peking University Third Hospital of Sports Medicine for patients with Achilles tendon rupture repair surgery

Description

Inclusion Criteria:

  • Rupture of Achilles tendon repair surgery experience

Exclusion Criteria:

  • hypertension
  • diabetes
  • Professional athlete
  • No blood lipid test results

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients undergoing repair of Achilles tendon rupture
Procedure: Repair surgery for Achilles tendon rupture
Repair surgery for Achilles tendon rupture
Subjects who underwent physical examination during the same period
Subjects who underwent physical examination in the Physical Examination Center of Peking University Third Hospital during the same period

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood glucose levels
Time Frame: a month after the surgery
Blood glucose levels of patients and control group were measured one month after surgery.
a month after the surgery
blood lipid levels
Time Frame: a month after the surgery
blood lipid levels of patients and control group were measured one month after surgery.
a month after the surgery
uric acid levels
Time Frame: a month after the surgery
uric acid levels of patients and control group were measured one month after surgery.
a month after the surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Peking University Third Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2019

Primary Completion (ACTUAL)

February 1, 2019

Study Completion (ACTUAL)

March 1, 2019

Study Registration Dates

First Submitted

June 25, 2021

First Submitted That Met QC Criteria

July 4, 2021

First Posted (ACTUAL)

July 14, 2021

Study Record Updates

Last Update Posted (ACTUAL)

July 14, 2021

Last Update Submitted That Met QC Criteria

July 4, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • M2019127

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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