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Maylard versus Cherney incision for gynecologic surgery

Maylard versus Cherney incision for gynecologic surgery : A double blind clinical controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210404050838N1
Enrollment
60
Registered
2021-11-30
Start date
2021-12-03
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Maylard and Cherney incision in gynecologic surgery.

Interventions

Intervention 1: Intervention group 1: Patients undergoing hysterectomy by Millard incision method Intervention group The operative p

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: Hysterectomies for benign con-ditions Ages 35-65 years

Exclusion criteria

Exclusion criteria: Abdominal wall hernia Poor control diabetes (hemoglobin A1C greater than 8) Systemic disease leading to corticosteroid therapy in the last six months Thrombophilia Problems Malignancies with diagnosis or chemo radiation in the last 6 months Body mass index more than 30 kg / m2 Smoking History of more than twice previous abdominal surgery Anticoagulant treatment

Design outcomes

Primary

MeasureTime frame
Volume of blood loss. Timepoint: From the beginning to the end of the surgery. Method of measurement: Counting used gases at the surgical site.;Duration of surgery. Timepoint: From the beginning to the end of the surgery. Method of measurement: Minute.

Secondary

MeasureTime frame
Abdominal dis-tension. Timepoint: From the end of surgery until 12 hours later. Method of measurement: Clinical examination.;The amount of pain after surgery. Timepoint: From the first to the third day of surgery twice a day (8 am and 4 pm). Method of measurement: Visual Analogue Scale.;Hematoma at the surgical site. Timepoint: The tenth day after surgery, then, every month, until three months after surgery. Method of measurement: Clinical examination.;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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Vaezi

Tabriz University of Medical Sciences

lahroudin@gmail.com+98 35519161

Outcome results

None listed

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