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Comparison of the effects of spinal anesthesia in pregnant women with and without diabetes during pregnancy undergoing cesarean delivery

Assessment oF Sensory and Motor Block Characteristics Following Spinal Anaesthesia in Parturients with Gestational Diabetes Mellitus Undergoing Cesarean Delivery: A Prospective Observational study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/07/114056
Enrollment
138
Registered
2026-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: O244- Gestational diabetes mellitus

Interventions

Intervention1: Gestational Diabetes Mellitus: Pregnant women diagnosed with Gestational Diabetes Mellitus Undergoing Cesarean Delivery under Spinal Anaesthesia Intervention2: Nil: Nil Control Interven

Sponsors

SRM Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA class 2 and 3, Gestational age greater than or equal to 37 weeks, Parturient who are undergoing elective or emergency LSCS under spinal anaesthesia, GDM diagnosed according to RCOG criteria for GDM group, Non diabetic parturients with normal glucose tolerance for control group

Exclusion criteria

Exclusion criteria: Lack of consent, Parturients with significant comorbidities other than GDM, Parturient who undergoing general anaesthesia.

Design outcomes

Primary

MeasureTime frame
Assessment of sensory and motor block characteristics following spinal anesthesia, including onset time, highest sensory block level, duration of sensory block regression to S2 dermatome, onset of motor block, and duration of motor block, recovery to Modified Bromage Scale Grade 0.Timepoint: Assessed from intrathecal injection until complete recovery of sensory block regression to S2 dermatome and motor block, Modified Bromage Scale Grade 0, with assessments at 3, 5, 10, 15, 30, 45, 60, 75, 90, and 105 minutes after spinal anesthesia, and continued postoperatively until complete block regression.—

Secondary

MeasureTime frame
Perioperative hemodynamic stability heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure, and Saturation, time to first postoperative analgesic requirement, and their association with block characteristics and clinical variables like BMI, glycemic control modality, and duration of surgery.Timepoint: Assessed from baseline before spinal anesthesia at 3, 5, 10, 15, 30, 45, 60, 75, 90, and 105 minutes after intrathecal injection, at the end of surgery, and continued postoperatively until the first analgesic requirement and complete sensory and motor block regression.—

Countries

India

Contacts

Public ContactMrs Swetha RK

SRM School of Allied Health Sciences

deepakmunusamy2023@gmail.com9361256359

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026