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Completed

NCT Number: NCT04960501

Comparison of Curative Effect Between New Tension Band and Patellar Tension Reduction Band in the Treatment of Lower Pole Fractures of Patella

Research purposes:

Analyze the curative effect of the new tension band system composed of φ3.0mm hollow nails, titanium cables and new gaskets and the patellar tension reduction band in the treatment of lower pole fractures of the patella.

research method: A retrospective study of 41 cases of comminuted fractures of the lower pole of the patella treated with a new tension band system composed of φ3.0mm hollow nails, titanium cables and new spacers from March 2012 to July 2017, including 19 males and 22 females , The average age is 56.7 years (22 to 79 years), 24 cases of AO/OTA A1 type, and 17 cases of C1.3 type. During the same period, 22 cases of comminuted fractures of the lower pole of the patella were treated with a patella tension band, including 8 males and 14 females, with an average age of 57.4 years (32 to 84 years), 17 cases of AO/OTA type A1, and 5 cases of type C1.3. The injury mechanism is all slipping and kneeling injuries.

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Key information

Age range

22 year–79 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Peking University Third Hospital

Beijing, Beijing Municipality, 100191, China

About this study

Research purposes:

Analyze the curative effect of the new tension band system composed of φ3.0mm hollow nails, titanium cables and new gaskets and the patellar tension reduction band in the treatment of lower pole fractures of the patella.

research method: A retrospective study of 41 cases of comminuted fractures of the lower pole of the patella treated with a new tension band system composed of φ3.0mm hollow nails, titanium cables and new spacers from March 2012 to July 2017, including 19 males and 22 females , The average age is 56.7 years (22 to 79 years), 24 cases of AO/OTA A1 type, and 17 cases of C1.3 type. During the same period, 22 cases of comminuted fractures of the lower pole of the patella were treated with a patella tension band, including 8 males and 14 females, with an average age of 57.4 years (32 to 84 years), 17 cases of AO/OTA type A1, and 5 cases of type C1.3. The injury mechanism is all slipping and kneeling injuries.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients with comminuted fractures of the lower pole of the patella: AO/OTA type A1 and C1.3 type -

Exclusion criteria

1. Except for other types of patella fractures 2. Except for open patella fractures 3. Excluding patients with other fractures and injuries 4. Exclude patients who cannot cooperate with functional exercises

-

Treatment and study plan

New type of tension band or patellar tension reduction band for treatment of lower pole fracture of patella

Procedure

New type of tension band or patellar tension reduction band for treatment of lower pole fracture of patella

Primary outcomes

  1. operation time

    Time frame: One day after surgery

Secondary outcomes

  1. Surgical bleeding

    Time frame: One day after surgery

Other outcomes

  1. Knee joint score after surgery

    Time frame: One week, one month, three months, six months after operation

  2. Postoperative X-ray

    Time frame: One week, one month, three months, six months after operation

  3. Follow-up body image data

    Time frame: One week, one month, three months, six months after operation

Sponsors and collaborators

Lead sponsor

Peking University Third Hospital

Other

Registry information

Important dates

Study start
2012
Primary completion
2012
Study completion
2017
First posted
Jul 14, 2021
Registry last updated
Jul 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.