NCT07887165

Brief Summary

This project intends to retrospectively review the medical records of patients with Haglund's syndrome who underwent surgical treatment in the Department of Sports Medicine and Joint Surgery between 2019 and 2026, to analyze the advantages and limitations of totalendoscopic calcaneoplasty combined with Achilles tendon insertion reconstruction compared with conventional open surgery. The findings are expected to provide scientific evidence for individualized treatment of patients with Haglund's syndrome.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
67

participants targeted

Target at P25-P50 for all trials

Timeline
2mo left

Started Nov 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 8, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

October 21, 2026

Completed
11 days until next milestone

Study Start

First participant enrolled

November 1, 2026

Expected
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

October 21, 2026

Status Verified

October 1, 2026

Enrollment Period

2 months

First QC Date

October 8, 2026

Last Update Submit

October 14, 2026

Conditions

Keywords

insertional Achilles tendinopathyHaglund Syndromeendoscopic calcaneoplasty

Outcome Measures

Primary Outcomes (3)

  • Victorian Institute of Sport Assessment-Achilles,VISA-A

    Evaluation of foot and ankle function. Higher scores indicate better function.

    pre-surgery, 1-month after the surgery, 3-month after the surgery, 6-month after the surgery, 12-month after the surgery

  • American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot Scale

    Evaluation of foot and ankle function. Higher scores indicate better function.

    pre-surgery, 1-month after the surgery, 3-month after the surgery, 6-month after the surgery, 12-month after the surgery

  • visual analogue scale,VAS

    The visual analogue scale (VAS) is a pain assessment scale, in which lower scores indicate less severe pain

    pre-surgery, 1-month after the surgery, 3-month after the surgery, 6-month after the surgery, 12-month after the surgery

Secondary Outcomes (5)

  • Fowler-Philip angle

    perioperatively、after the surgery

  • Height of Haglund deformity

    perioperatively、after the surgery

  • BMI

    baseline

  • Calcaneal X/Y ratio

    perioperatively、after the surgery

  • age

    baseline

Study Arms (2)

OPEN

Patients with Haglund syndrome and insertional Achilles tendinopathy treated with open calcaneoplasty.

ENDO

Patients with Haglund syndrome and insertional Achilles tendinopathy treated with endoscopic calcaneoplasty combined with insertional Achilles tendon reconstruction.

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients diagnosed with Haglund syndrome and insertional Achilles tendinopathy who received surgical treatment in our hospital. Subjects were retrospectively screened according to inclusion and exclusion criteria and divided into two groups based on surgical approach. Both groups underwent calcaneoplasty combined with insertional Achilles tendon reconstruction, one via open approach and the other via endoscopic approach.

You may qualify if:

  • : Patients had completed at least 12-month postoperative follow-up
  • : Complete medical records and imaging findings were available

You may not qualify if:

  • : Patients with previous Achilles tendon surgery.
  • : Patients with missing medical records or imaging findings that precluded valid evaluation.
  • : Patients deemed ineligible for enrollment by the investigators for other reasons.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Joint and Sports Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, China

Nanjing, Jiangsu, 210000, China

Location

Central Study Contacts

Yiqiu Jiang, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief Physician

Study Record Dates

First Submitted

October 8, 2026

First Posted

October 21, 2026

Study Start (Estimated)

November 1, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

October 21, 2026

Record last verified: 2026-10

Data Sharing

IPD Sharing
Will not share

Locations