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

Risk Factors and a Predictive Nomogram for Acute Moderate-to-severe Postoperative Pain Afte Achilles Tendon Surgery: A Retrospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07558512
Enrollment
489
Registered
2026-04-30
Start date
2026-04-16
Completion date
2026-04-25
Last updated
2026-05-08

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

Conditions

Postoperative Pain

Brief 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.

Interventions

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

Min Li
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

1. Age ≥ 18 years; American Society of Anesthesiologists (ASA) physical status classification Ⅰ\~Ⅲ; 2. Clinically diagnosed with Achilles tendon rupture, Achilles tendinopathy, insertional Achilles tendinitis, Haglund's deformity, or other Achilles tendon disorders; 3. Undergoing open or arthroscopic Achilles tendon surgery; 4. Conscious and able to cooperate in surgery and postoperative pain assessment; 5. Complete and accessible case data related to surgery, anesthesia, and postoperative pain assessment; 6. Completion of at least 24 hours of standardized pain monitoring and clinical follow-up after surgery

Exclusion criteria

1. Missing or incomplete key clinical data such as pain assessment, surgery and anesthesia; 2. Failure to complete 24-hour standardized pain monitoring after surgery; Perioperative unplanned secondary surgery or transfer to the intensive care unit (ICU); 3. Patients with mental illness, cognitive dysfunction, or language communication barrier; History of alcohol or drug addiction Pain due to other acute or chronic diseases; 4. Bilateral Achilles tendon surgery Concurrent surgery for other lower extremity injuries

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Moderate-to-Severe Acute Postoperative PainWithin 24 hours after surgeryDefined as a pain score ≥ 4 on the Numeric Rating Scale (NRS) or the need for rescue analgesia within the first 24 hours after Achilles tendon surgery. The NRS is an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain), where higher scores indicate greater pain severity (worse outcome).

Secondary

MeasureTime frameDescription
Highest Postoperative Pain ScoreWithin 24 hours after surgeryThe maximum pain score recorded within 24 hours after Achilles tendon surgery, measured using the Numeric Rating Scale (NRS). The NRS is an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain), where higher scores indicate greater pain severity (worse outcome).
Rescue Analgesia RequirementWithin 24 hours after surgeryProportion of patients requiring rescue analgesic medications within 24 hours after surgery.
Incidence of Postoperative Nausea and Vomiting (PONV)Within 24 hours after surgeryProportion of patients experiencing nausea or vomiting requiring antiemetic treatment within 24 hours after surgery.
Postoperative Length of Hospital StayFrom surgery to hospital discharge (up to 7 days)Number of days from surgery to hospital discharge.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026