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Risk Factors and a Predictive Nomogram for Acute Moderate-to-severe Postoperative Pain After Achilles Tendon Surgery

NCT07558512 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 489

Last updated 2026-05-08

No results posted yet for this study

Summary

This is a single-center retrospective cohort study to identify independent risk factors and develop a predictive nomogram for moderate-to-severe pain within 24 hours after Achilles tendon surgery.

Conditions

  • Postoperative Pain

Interventions

OTHER

No Study-Specific Intervention

This is a retrospective observational cohort study. No study-specific intervention is being investigated; all patients received routine clinical care as per standard practice.

Sponsors & Collaborators

  • Min Li

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-16
Primary Completion
2026-04-25
Completion
2026-04-25

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07558512 on ClinicalTrials.gov