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Two different surgical techniques to close thoracotomy incision to decrease the pain after surgery

Determination the severity (rate) of pain after closing thoracotomy incision by intracostal sutures and pericostal sutures

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015080323480N1
Enrollment
134
Registered
2016-02-09
Start date
2016-02-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

injury of intercostal nerves. injury of other nerves of thorax

Interventions

Intervention 1: Intervention group 1: patients are their chests closed with pericostal sutures (stitches are placed on top of the fifth rib and on top of the seventh rib). Intervention 2: Interventio
Prevention
Intervention group 1: patients are their chests closed with pericostal sutures (stitches are placed on top of the fifth rib and on top of the seventh rib).
Intervention group 2: patients are their chest closed with intracostal sutures (stitches will place on top of the fifth rib and through the small holes drilled in the bed of the sixth rib).

Sponsors

Vice Chancellor for research of Qom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with thoracotomy indication. The exclusion criteria: patients younger than 19 years and older than 100 years; chronic pain; long-term use of nonsteroidal anti-inflammatory drugs (NSAIDs) or analgesics; psychiatric illness; cancer invasion into the chest wall; preoperative chest radiation or chemotherapy; previous ipsilateral thoracotomy; neurological diseases such as diabetes-related neuropathy; a history of a previous ipsilateral thoracotomy; rib fracture during surgery; incision infection or empyema; loss of consciousness; mechanical ventilator assistance; pulmonary embolism; reoperation and Patients unwillingness to continue the trial.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 3 days after surgery. Method of measurement: numeric pain rating score.

Secondary

MeasureTime frame
Air lea; hemorrahge; pneumonia; emboli and DVT; empyema; wound infection; atelectasis. Timepoint: every day after surgery. Method of measurement: physical examination and history taking; CXRay.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hossein Ghasem Begloo

Qom University of Medical Sciences

mghasembegloo@yahoo.com+98 25 3612 2000

Outcome results

None listed

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