study Comparison Of Spinal Anesthesia And Segmental spinal Anesthesia In Abdominal Surgery

Comparison Of Spinal Anesthesia And Segmental spinal Anesthesia In Abdominal Surgery - A Prospective, Randomised , Comparative, Clinical Study - Nil

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/075820

Enrollment

Registered

2024-10-24

Start date

Unknown

Completion date

Unknown

Last updated

2025-11-17

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

Conditions

Health Condition 1: K40- Inguinal hernia Health Condition 2: K31- Other diseases of stomach and duodenum Health Condition 3: K41- Femoral hernia Health Condition 4: K42- Umbilical hernia Health Condition 5: K45- Other abdominal hernia

Interventions

Intervention1: spinal anaesthesia: spinal anaesthesia with hyperbaric bupivacaine in moderate duration abdominal sugeries Intervention2: Segmental Spinal anaesthesia: Segmental Spinal anaesthesia with

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18 to 60 years ? Patients undergoing open abdominal surgeries under spinal anesthesia (SA) or segmental spinal anesthesia (SSA). Sex - male and female. Patients who can understand the rate of their pain on visual analog scale(VAS) or pain Patients who could provide written informed consent. Open abdominal surgeries of moderate duration (60 - 120 minutes)

Exclusion criteria

Exclusion criteria: Patients refusal to consent. Pregnant women Patients with history of allergy to local anesthetic agents. Presence of pain or infection over the injection site Patients having significant neurological disease with motor or sensory deficit Any contraindication to spinal anesthesia.

Design outcomes

Primary

Measure	Time frame
1. To compare hemodynamic parameters like heart-rate, blood pressure, mean arterial pressure, oxygen saturation. 2. To compare the onset of surgical anesthesia. 3. To compare duration of action for sensory and motor block 4. To compare adequacy of abdominal relaxation 5. To compare the post operative VAS score. 6. To compare the time for first voiding 7. To compare time for ambulation of patients.Timepoint: Preoperative intraoperative and post operative 24 hours after the surgery	—

Measure

Time frame

1. To compare hemodynamic parameters like heart-rate, blood pressure, mean arterial pressure, oxygen saturation. 2. To compare the onset of surgical anesthesia. 3. To compare duration of action for sensory and motor block 4. To compare adequacy of abdominal relaxation 5. To compare the post operative VAS score. 6. To compare the time for first voiding 7. To compare time for ambulation of patients.Timepoint: Preoperative intraoperative and post operative 24 hours after the surgery

—

Secondary

Measure	Time frame
To compare the time for first voiding and to compare time for ambulation of patients.Timepoint: From end of surgery to 24hours after the surgery	—

Countries

India

Contacts

Public ContactDr Minal Harde

Topiwala National Medical College and Dr B.Y.L. Charitable Hospital.

minalharde@gmail.com2223027137

Outcome results

None listed

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