An exploratory study for the improvement of abdominal muscle function in female patients with abdominal wall surgery by preoperative abdominal muscle exercise

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900023012

Enrollment

Unknown

Registered

2019-05-07

Start date

2019-06-01

Completion date

Unknown

Last updated

2019-05-13

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

Conditions

Hernia

Interventions

1:Rehabilitation exercise

2:No rehabilitation exercise

Eligibility

Sex/Gender

Female

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) female patients with abdominal incisional hernia should refer to the European classification standards for incisional hernia. (2) aged 18-75 years. (3) duration of incisional hernia disease < 5 years. (4) surface emg examination indicated abnormal spontaneous electrical activity of the muscles in the resting state of the anterior abdominal wall. (5) elastic ultrasound examination indicated the existence of anterior abdominal wall muscle groups (external abdominal oblique, internal abdominal oblique, transverse abdominal muscle). (6) sign the informed consent;

Exclusion criteria

Exclusion criteria: (1) elastic ultrasound indicated muscle fibrosis; (2) combined with central and peripheral nervous system diseases; (3) combined with musculoskeletal diseases; (4) tumor recurrence; (5) history of pacemaker installation; (6) patients and their families have poor compliance, and cannot cooperate with clinical treatment and follow-up; (7) chronic diseases are not well controlled; (8) pregnancy, lactation or intention to become pregnant during the study period; (9) infection or skin disease occurs at the abdomen rehabilitation site; (10) previous radiation therapy; (11) severe obstructive pulmonary disease or severe restrictive pulmonary disease; (FEV1 is normal or larger than FVC, and VC is accounted for estimated percentage for 10 years; (16) recurrent hernia, previous history of mesh implantation; (17) refractory hernia, incarcerated hernia and strangulated hernia; (18) other circumstances in which the investigator considers the patient to be unfit to participate in the clinical trial.

Design outcomes

Primary

Measure	Time frame
Evaluation of Rehabilitation Comprehensive Scale;Assessment of abdominal wall function;	—

Secondary

Measure	Time frame
Recurrence rate;	—

Countries

China

Contacts

Public ContactHe Kai

Department of General Surgery, Huashan Hospital

hekai1025@qq.com+86 13816422298

Outcome results

None listed

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