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Outcome of Two Different Suture Methods for Achilles Tendon Rupture

Closed Achilles Tendon Rupture Treats by Two Different Suture Methods and the Outcome

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01622179
Enrollment
40
Registered
2012-06-19
Start date
2012-06-30
Completion date
2013-06-30
Last updated
2013-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Achilles Tendon Rupture

Keywords

surgery, suture method, blood supply

Brief summary

The purpose of this study is to estimate the effective of two suture methods in the treatment of Achilles rupture.

Detailed description

Achilles tendon rupture is one of the most common tendon injuries in the adult population. The incidence of this injury is increasing as aging adults continue their participation in high-demand sports. Although the impact of an Achilles tendon rupture is substantial, often resulting in prolonged disability and rehabilitation. Studies have showed that the operation treatment of acute Achilles tendon ruptures had some advantages. But the rebuild of blood supply was not involved in previous studies. And the epitenon of tendon is the interior layer, closest to the endotenons which contains the vascular supply. Main difference of two suture methods were if the epitenon was repaired and sewed indirectly or unrepaired and sewed directly.

Interventions

PROCEDUREsewed indirectly

The epitenon was repaired and sewed indirectly.

PROCEDUREsewed directly

The epitenon was unrepaired and sewed directly.

Sponsors

Peifu Tang
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Adult men or women between 18 and 60 years of age. * Closed rupture confirmed with ultrasound or magnetic resonance imaging (MRI). * Operative within 14 days after injury. * Willing and able to comply with and carry out the prescribed rehabilitation protocol. * Providing informed consent. * No other major trauma.

Exclusion criteria

* Refuse to participate. * Refuse to participate. * Additional ipsilateral injury. * Open injury. * Patients not suitable for surgery (i.e., mellitus diabetes, immunocompromised states, obesity (BMI.30), peripheral vascular disease or local/systemic dermatologic disorders) or have other surgical contraindications. * Fluoroquinolone-associated rupture (i.e., rupture within 2 weeks after taking this medication). * Achilles avulsion from the calcaneus or with bone fracture. * Neurological or vascular disease requiring medications recognized to impair tendon healing.

Design outcomes

Primary

MeasureTime frameDescription
Blood supply conditionsix weeksBlood supply was estimated by ultrasonic contrast at six weeks after surgery.

Secondary

MeasureTime frameDescription
Calf circumferencesix weeksCalf circumference was measured at six weeks after surgery.
Complicationssix monthsInfection and rerupture at six month after surgery.

Countries

China

Contacts

Primary ContactTang P Fu, Dr.
pftang301@126.com861099638101
Backup ContactZhang L Hai, Dr.
zhanglihai74@yahoo.com.cn861099638102

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026