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Not yet recruitingNCT07887165Updated Oct 21, 2026

Open Versus Fully Endoscopic Calcaneoplasty With Achilles Tendon Insertional Reconstruction for Haglund Syndrome

An observational study in Haglund Syndrome and Insertional Achilles Tendinopathy, sponsored by Nanjing First Hospital, Nanjing Medical University. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Nanjing First Hospital, Nanjing Medical University · Observational

Updated Oct 21, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
67
Ages
18 Years to 80 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Haglund Syndrome
  • Insertional Achilles Tendinopathy

Keywords

  • insertional Achilles tendinopathy
  • Haglund Syndrome
  • endoscopic calcaneoplasty
03

In context

Lead sponsor

Nanjing First Hospital, Nanjing Medical University is the lead sponsor of 220 studies on the registry; 107 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-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.

Eligibility criteria

Inclusion Criteria:1: Patients attended the orthopedic outpatient clinic of Nanjing First Hospital and underwent open or endoscopic calcaneoplasty combined with Achilles tendon insertion reconstruction between 2019 and 2026.

2: Patients had completed at least 12-month postoperative follow-up

3: Complete medical records and imaging findings were available

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Exclusion Criteria:1: Patients with severe Achilles tendon injury or complete rupture.

2: Patients with previous Achilles tendon surgery.

3: Patients with missing medical records or imaging findings that precluded valid evaluation.

4: Patients deemed ineligible for enrollment by the investigators for other reasons.

-

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
67 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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.

06

What researchers measure

Primary outcomes

  1. Victorian Institute of Sport Assessment-Achilles,VISA-A

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

    Time frame: pre-surgery, 1-month after the surgery, 3-month after the surgery, 6-month after the surgery, 12-month after the surgery

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

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

    Time frame: pre-surgery, 1-month after the surgery, 3-month after the surgery, 6-month after the surgery, 12-month after the surgery

  3. visual analogue scale,VAS

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

    Time frame: pre-surgery, 1-month after the surgery, 3-month after the surgery, 6-month after the surgery, 12-month after the surgery

Secondary outcomes

  1. Fowler-Philip angle

    The Fowler-Philip angle was measured on radiographic images in degrees

    Time frame: perioperatively、after the surgery

  2. Height of Haglund deformity

    The Height of Haglund deformity was measured on radiographic images in mm

    Time frame: perioperatively、after the surgery

  3. BMI

    weight and height will be combined to report BMI in kg/m\^2

    Time frame: baseline

  4. Calcaneal X/Y ratio

    The Calcaneal X/Y ratio was measured on radiographic images

    Time frame: perioperatively、after the surgery

  5. age

    age

    Time frame: baseline

07

Study locations

1 site
  • Department of Joint and Sports Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, China
    Nanjing, Jiangsu 210000, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Dec 2026, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 8, 2026
First posted
Oct 21, 2026
StartEst.
Nov 1, 2026
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2026
Last update
Oct 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07887165
Responsible party
Yiqiu Jiang (Chief Physician, Nanjing First Hospital, Nanjing Medical University) — Principal investigator
First posted
Oct 21, 2026
Start date
Nov 1, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Oct 21, 2026

Study contacts

Yiqiu Jiang, MD, PhD
Contact
jyq_3000@163.com
86+15861819900

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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