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Effects of preoperative depression with scoliosis on postoperative acute and chronic pain and prognosis in adolescents: a single-center, observational and prospective cohort study

Effects of preoperative depression with scoliosis on postoperative acute and chronic pain and prognosis in adolescents: a single-center, observational and prospective cohort study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077637
Enrollment
Unknown
Registered
2023-11-14
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

Adolescent Scoliosis

Interventions

Depression group:None
Non-depressive group :None

Sponsors

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1.Age = 10 years and Age <18 years 2.Proposed elective scoliosis orthopedic surgery 3.ASA classification (American Association of Anesthesiologists) is grade I-III 4.Agreed to participate in this study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Refuse to participate in this study; 2. There is acute and chronic pain before surgery. 3 History of the use of long-term oral analgesics and opioid analgesics before surgery; 4 Severe liver dysfunction (Child-Pugh C), renal dysfunction (preoperative dialysis) or expected survival =24 hours of patients; 5 Preoperative schizophrenia, bipolar disorder, epilepsy, myasthenia gravis; 6 Unable to communicate before surgery due to coma, severe dementia, speech impairment or severe hearing impairment; 7 Preoperative severe hypertension, sinus tachycardia, acute coronary syndrome within 1 week, severe heavy intracranial hypertension; 8 Refuse to use the postoperative self-controlled analgesic pump; 9 Use of ketamine/ E-sketamine during surgery 10. Those who is participating in other interventional clinical studies

Design outcomes

Primary

MeasureTime frame
Moderate and severe pain (NRS);

Secondary

MeasureTime frame
Depression score (CDI);Pain score (NRS);Orthopedic condition score (SRS-22);Quality of life score (SF-36);Sleep score (NRS);Cognitive function score;The type, frequency and dosage of analgesic drugs;Occurrence of delirium;30days after surgery(survival or death);Complication;postoperative hospitalization;

Countries

China

Contacts

Public ContactBo Jinhua

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School2023-

bojinhua@njglyy.com+86 159 5198 7578

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 29, 2026