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Application of Transcutaneous Electrical Acupoint Stimulation Combined with Ultrasound-Guided Thoracolumbar Interfascial Plane Block in Children with Cerebral Palsy undergoing Selective Posterior Rhizotomy

Application of Transcutaneous Electrical Acupoint Stimulation Combined with Ultrasound-Guided Thoracolumbar Interfascial Plane Block in Children with Cerebral Palsy undergoing Selective Posterior Rhizotomy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061543
Enrollment
Unknown
Registered
2022-06-28
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Cerebral Palsy

Interventions

Group B:General anesthesia combined with TLIP block
Group E:General anesthesia combined with TEAS
Group EB:General anesthesia combined with TEAS and TLIP block

Sponsors

Dongzhimen Hospital, Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Children undergoing SPR surgery under general anesthesia; 2. Children aged 6 to 12 years old, no gender limitations; 3. ASA grade I to II.

Exclusion criteria

Exclusion criteria: 1. Severe spinal deformity; 2. Secondary or above lumbar surgery; 3. Puncture site infection, rupture; 4. Allergy to local anesthetics; 5. Coagulation abnormalities; 6. Serious cardiopulmonary disease; 7. Liver and kidney function abnormal; 8. Children with mental retardation or mental illness; 9. Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
VAS (Visual analog scale) during rest;VAS (Visual analog scale) during movement;m-CHEOPS (Modified Children's Hospital of Eastern Ontario Pain Scale);The 15-Item Quality of Recovery score scale;Level of sedation;PAED (Pediatric anesthesia emergence delirium scale) score;Perioperative hemodynamics;Intraoperative remifentanil and propofol dosage;The pressing times of PCIA pump;Consumption of analgesic drugs;

Secondary

MeasureTime frame
Operation time;Postoperative hospital stay;Patients and their family members satisfaction;Rate of adverse reactions;

Countries

China

Contacts

Public ContactHuilong Ren

Dongzhimen Hospital, Beijing University of Chinese Medicine

18612923335@163.com+86 18612923335

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026