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A study to know the effect of instillation of local anesthetic agent ,bupivacaine in abdomen for relief of pain after cesarean section

Effectiveness of intraperitoneal instillation plus infiltration of bupivacaine as an analgesic for postoperative pain relief in LSCS.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/01/007679
Enrollment
100
Registered
2017-01-11
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: null- Primi gravida,of ASA grade 1 or2,aged between20 to 40 years, posted for planned or emergency cesarean section under spinal anesthesia

Interventions

Intervention1: Bupivacaine (0.25%)-40 ml.: 20 ml of bupivacaine(0.25%) instillation intrapertionealy and 20 ml of bupivacaine (0.25%) infiltration in subcutaneous tissue at stich site one time during

Sponsors

Government medical college surat
Lead Sponsor
DrRohit Garg
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Primigravida posted for planned or emergency cesarean section under spinal anesthesia. 2.Patient who comes under ASA class 1 & 2 and age having between 20 yrs to 40 yrs.

Exclusion criteria

Exclusion criteria: 1.Patient having previous abdominal surgery. 2.patient giving negative consent for this procedure. 3.patient allergic to bupivacaine.

Design outcomes

Primary

MeasureTime frame
TO evaluate the duration of analgesia by bupivacaine (0.25%) instillation plus infiltration after cesarean section. 2.Total requirement of other analgesic agent in 24 hours after cesarean section.Timepoint: Time when patient first ask for analgesic agent. 24 hours after giving spinal anesthesia.

Secondary

MeasureTime frame
1.To study the side effect which may occurs following instillation plus infiltration of bupivacaine (0.25%). 2.To evaluate the patient satisfaction for pain relief after cesarean section.Timepoint: during 24 hours after spinal anesthesia

Countries

India

Contacts

Public ContactDr Harsha Patel

Government Medical College Surat

harshapad@yahoo.com9925176299

Outcome results

None listed

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