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A study to compare staples non dissolvable sutures versus subcuticular dissolvable sutures for skin closure in caesarean section

Comparison of staples versus subcuticular sutures for skin closure in caesarean section-A Randomized controlled study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025555
Enrollment
289
Registered
2020-06-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O754- Other complications of obstetric surgery and procedures

Interventions

Intervention1: metallic surgical skin staplers: subcuticular sutures vs metallic skin staplers for skin closure in cesarean section Control Intervention1: subcuticular sutures: subcuticular sutures v

Sponsors

AIIMS JODHPUR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Women with viable pregnancies (>= 26 weeks) undergoing caesarean delivery at AIIMS, Jodhpur. 2. All caesarean types will be included - scheduled or unscheduled and primary or repeat caesareans with low transverse/ Pfannenstiel incision

Exclusion criteria

Exclusion criteria: 1. Inability to obtain informed consent 2. Immune compromising disease (e.g. AIDS) 3. Chronic steroid use 4. Contraindication to routine postpartum pain medications (ibuprofen,narcotics) eg in CKD patient 5. Chorioamnioinitis 6. Caesarean section done by vertical incision.

Design outcomes

Primary

MeasureTime frame
1.To compare the rate of wound complication by 6 weeks post operatively following metallic surgical stapler vs subcuticular sutures for skin closure after caesarean delivery Timepoint: day 3 post op 6 weeks post op

Secondary

MeasureTime frame
1. To compare the pain score post operatively on day 3 and after 6 weeks between metallic surgical staples and subcutaneous sutures skin closure after caesarean delivery 2.To compare the skin closure time between the two groups 3. To compare patient satisfaction rates between the two groups Timepoint: day 3 post op 6 weeks post op

Countries

India

Contacts

Public ContactShafaq Bhandari

All India Institute of Medical Sciences, Jodhpur

drmanu_8@yahoo.co.in9878828814

Outcome results

None listed

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