Comparison Maylard and Midline incision in patients with prior abdominal operation in major gynecologic surgeries

Comparison Maylard and Midline incision in patients with prior abdominal operation in major gynecologic surgeries - a clinical trial-

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220930056059N3

Enrollment

Registered

2026-04-11

Start date

2026-05-22

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

Major gynecological surgery. Acquired absence of both cervix and uterus

Interventions

Intervention 1: Intervention group 1: Patients undergoing hysterectomy by Maylard incision method Intervention group The operative procedure was similar and followed the same technical steps in both g

Eligibility

Sex/Gender

Female

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: women undergoing major surgery With a history of at least one and a maximum of three previous laparotomy In the age range of 20-60 years

Exclusion criteria

Exclusion criteria: Diabetes Presence of hernia in the abdominal wall known thrombophilia problems Patients treated with anticoagulants Cancers Body mass index more than 35 kg/m2 and smoking Smoking

Design outcomes

Primary

Measure	Time frame
Duration of surgery. Timepoint: From the beginning to the end of the surgery. Method of measurement: Digital timer.;Volume of blood loss. Timepoint: From the beginning to the end of the surgery. Method of measurement: Counting used gases at the surgical site.;Abdominal dis-tension. Timepoint: From the end of surgery until 12 hours later. Method of measurement: Clinical examination.;Intensity of pain. Timepoint: Twice daily (8 am and 4 pm) from the first to the third day of surgery. Method of measurement: Visual Analogue Scale of pain.	—

Measure

Time frame

Duration of surgery. Timepoint: From the beginning to the end of the surgery. Method of measurement: Digital timer.;Volume of blood loss. Timepoint: From the beginning to the end of the surgery. Method of measurement: Counting used gases at the surgical site.;Abdominal dis-tension. Timepoint: From the end of surgery until 12 hours later. Method of measurement: Clinical examination.;Intensity of pain. Timepoint: Twice daily (8 am and 4 pm) from the first to the third day of surgery. Method of measurement: Visual Analogue Scale of pain.

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Secondary

Measure	Time frame
Hematoma at the surgical site. Timepoint: The tenth day after surgery, then, every month, until three months after surgery. Method of measurement: Clinical examination.;Readmission due to surgical complications. Timepoint: Three months after surgery. Method of measurement: Questionnaire.;Surgical site infection. Timepoint: The tenth day after surgery, then, every month, until three months after surgery. Method of measurement: Clinical examination.;Surgical wound Opening. Timepoint: The tenth day after surgery, then, every month, until three months after surgery. Method of measurement: Clinical examination.	—

Measure

Time frame

Hematoma at the surgical site. Timepoint: The tenth day after surgery, then, every month, until three months after surgery. Method of measurement: Clinical examination.;Readmission due to surgical complications. Timepoint: Three months after surgery. Method of measurement: Questionnaire.;Surgical site infection. Timepoint: The tenth day after surgery, then, every month, until three months after surgery. Method of measurement: Clinical examination.;Surgical wound Opening. Timepoint: The tenth day after surgery, then, every month, until three months after surgery. Method of measurement: Clinical examination.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Maryam Vaezi

Tabriz University of Medical Sciences

mva260@yahoo.com+98 41 3551 9161

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026