Investigating the Efficacy of iTBS in Pain Management Post Laparoscopic Surgery as well as the Modulating Impact by Stimulation Targets: A Double-Blind, Sham-Controlled Clinical Trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100046324

Enrollment

Unknown

Registered

2021-05-14

Start date

2020-11-01

Completion date

Unknown

Last updated

2021-12-21

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

Conditions

Laparoscopic Surgery

Interventions

M1:iTBS over M1

DLPFC:iTBS over DLPFC

SHAM:SHAM

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70-years; 2. will undergo a laparoscopic surgery in 24 hours; 3. ASA level I-II.

Exclusion criteria

Exclusion criteria: 1. Cannot receive TMS (see screening criteria at Rossi et al., 2011); 2. Mental disorders assessed by MINI (Sheehan and Lecrubier, 2001); 3. Suicide ideation; 4. History of epilepsy; 5. Substance dependence.

Design outcomes

Primary

Measure	Time frame
PCA pump usage;	—

Secondary

Measure	Time frame
Pain intensity;	—

Countries

China

Contacts

Public ContactXianwei Che

Hangzhou Normal University

xianwei.che@hznu.edu.cn+86 18072852895

Outcome results

None listed

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