The Comparison of the Outcomes between Simple Hybrid VS Conventional Double Row Achilles Reattachment in Haglund Surgery

The Comparison of the Outcomes between Simple Hybrid VS Conventional Double Row Achilles Reattachment in Haglund Surgery : A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

TCTR

Registry ID

TCTR20251124020

Enrollment

Registered

2025-11-24

Start date

2025-11-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

outcome in Haglund Syndrome achilles reattachment technique Haglund Syndrome Simple hybrid reattachment double row suture single row suture pain functional outcome quality of life

Interventions

The Simple Achilles Hybrid Reattachment technique is a novel method for reattaching the Achilles tendon using only one suture anchor and one SwiveLock anchor. This technique was developed as a modific

Experimental Procedure/Surgery,Active Comparator Procedure/Surgery

Simple Achilles Reattachment,Double Row Suture

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Haglund syndrome patients aged over 18 years with who have failed nonoperative treatments, such as Achilles tendon stretching exercises, soft tissue massage at the painful area, and appropriate footwear modification for more than 3 months

Exclusion criteria

Exclusion criteria: 1. Patients with a history of previous Achilles tendon injury or rupture. 2. Patients unable to comply with postoperative rehabilitation protocols. 3. Patients with skin or soft tissue infection around the foot or ankle within the past 3 months. 4. Patients with concomitant foot or ankle deformities. 5. Patients with incomplete medical records or radiographic data within 3 months prior to surgery. 6. Patients presenting with unilateral or bilateral lower limb weakness from any cause. 7. Patients undergoing revision surgery for posterior calcaneal exostosis (heel spur).

Design outcomes

Primary

Measure	Time frame
Pain at 3 months and 6 months postoperative Visual Analogue Scale	—

Secondary

Measure	Time frame
Function at 3 months and 6 months postoperative Patient reported outcome using a questionnaire interview using FAAM for ADL (Foot and Ankle Ability Measure Activities of Daily Living) ,Quality of life at 3 months and 6 months postoperative Patient reported outcome using a questionnaire interview using SF-36,Plantar flexion strength at 3 months and 6 months postoperative Categorical data by using single heel rise test,Hospital Cost after patient was discharged from the hospital Cost in an admission using hospital billing record,Complication Until 6 months postoperative Not statistical method	—

Measure

Time frame

Function at 3 months and 6 months postoperative Patient reported outcome using a questionnaire interview using FAAM for ADL (Foot and Ankle Ability Measure Activities of Daily Living) ,Quality of life at 3 months and 6 months postoperative Patient reported outcome using a questionnaire interview using SF-36,Plantar flexion strength at 3 months and 6 months postoperative Categorical data by using single heel rise test,Hospital Cost after patient was discharged from the hospital Cost in an admission using hospital billing record,Complication Until 6 months postoperative Not statistical method

—

Countries

Thailand

Contacts

Public ContactThos Harnroongroj

Faculty of medicine, Siriraj hospital, Mahidol university

ultradeutsch@gmail.com024197965

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026