Ultrasound Guided Rectus Sheath Block Versus Intrathecal Morphine for Postoperative Analgesia in Patients Undergoing Open Total Abdominal Hysterectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorAin Shams University

About this trial

This study aims to compare the effectiveness and safety of ultrasound-guided rectus sheath block versus intrathecal morphine for postoperative analgesia in patients undergoing open total abdominal hysterectomy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age: 18 - 65 years old.

American Society of Anesthesiologists (ASA) physical status (I -II).

Patients undergoing open total abdominal hysterectomy.

Disqualifiers

Hepatic, renal, or cardiac disease.

Any known allergy to local anesthetic.

Physical or mental conditions which may vague measuring postoperative pain following surgery.

History of chronic use of analgesic as nonsteroidal anti-inflammatory drugs (NSAIDs) or central nervous system (CNS) depressants as antiepileptic, and bleeding disorders.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Rectus sheath block

    Drug

    Patients will receive rectus sheath block (20 ml bilaterally, bupivacaine 0.25%) after induction of general anesthesia.

  • Intrathecal morphine

    Drug

    Patients will receive 150 µg intrathecal morphine after induction of general anesthesia.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Rectus sheath block groupExperimental treatment 1 intervention
Group B: Intrathecal morphine groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Total morphine consumption

Morphine will be administered if the visual analog scale (VAS) score is ≥ 4.

Time frame
24 hours postoperatively

Secondary outcomes

1

Time to the first request for the rescue analgesia

Time to the first request for the rescue analgesia (time from the end of surgery till first dose of morphine administrated)

Time frame
24 hours postoperatively
2

Degree of pain

Each patient will be instructed about postoperative pain assessment with the Visual Analogue Scale (VAS). VAS (0 represents "no pain" while 10 represents "the worst pain imaginable"). VAS will be assessed after surgery over 24 hour using VAS scale at (post-anesthesia care unit, 2, 4, 6, 12, 18, and 24 h).

Time frame
24 hours postoperatively
3

Degree of sedation

Sedation will be assessed using Modified Observer's Assessment of Alertness/Sedation Scale (MOAA/S): (5 Alert: Responds readily to name spoken in normal tone, 4: Lethargic response to name spoken in normal tone, 3: Responds only after name is called loudly and/or repeatedly, 2: Responds only after mild prodding or shaking ,1: Responds only after painful trapezius squeeze,0: Does not respond to painful trapezius squeeze).

Time frame
Intraoperatively
4

Degree of patient satisfaction

The degree of patient satisfaction will be assessed on a 5-point Likert scale patient satisfaction (1, extremely dissatisfied; 2, unsatisfied; 3, neutral; 4, satisfied; 5, extremely satisfied).

Time frame
24 hours postoperatively

Other outcomes

Sponsors and contacts

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