Impact of Ketamine On Depressive Symptoms In Patients Undergoing Lumbo-peritoneal Shunt Insertion

Sponsor
Benha University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06060210
Collaborator
(none)
60
1
2
6.1
9.9

Study Details

Study Description

Brief Summary

Postoperative depression is a perioperative psychological complication that severely affects patient recovery and quality of life. In extreme cases, it may lead to suicidal behavior. Postoperative depression can be seen in various surgical operations .

High rates of anxiety and depression have been reported in cohorts of patients with IIH, though it is not clear whether there is any direct relationship. Worse outcomes in terms of disability level and symptom resolution have been observed in IIH patients who have a known co-existing psychiatric illness compared to those who do not .

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Postoperative depression is a perioperative psychological complication that severely affects patient recovery and quality of life. In extreme cases, it may lead to suicidal behavior. Postoperative depression can be seen in various surgical operations.

Idiopathic intracranial hypertension (IIH) is the most common cause of papilledema and is typically seen in young women with elevated body mass index. The prevalence of IIH has been increasing in recent years, in parallel with climbing rates of obesity .

High rates of anxiety and depression have been reported in cohorts of patients with IIH, though it is not clear whether there is any direct relationship. Worse outcomes in terms of disability level and symptom resolution have been observed in IIH patients who have a known co-existing psychiatric illness compared to those who do not .

The use of lumbo-peritoneal (LP) shunts has been well documented as a treatment modality for patients with idiopathic intracranial hypertension (IIH). There are a number of advantages to LP shunts when compared with other treatment modalities for IIH, such as stereotactic ventriculo-peritoneal shunts (VP) and optic nerve sheath fenestrations (ONSF). LP shunts avoid intracranial risks, such as cerebral hemorrhage, seizures, and shunt malposition.

Over the past decade, it has been provoked a single administration of ketamine elicits fast (in as little as half an hour) and sustained antidepressant effects both in human and animal models of depression. There are some potential mechanisms of antidepressant actions of ketamine. MK-801, a noncompetitive NMDA receptor antagonist, produced antidepressant-like actions in the animal model of depression . Ketamine can also increase hippocampal brain-derived neurotrophic factor levels, which may be important for producing a rapid onset of antidepressant action .A recent study found ketamine could quickly elevate mood by blocking NMDAR receptor-dependent bursting activity of the lateral habenula neurons to disinhibit downstream monoaminergic reward centers and provide a framework for developing new rapid-acting antidepressants .

Accordingly, we hypothesized that intraoperative ketamine can reduce the post operative depressive symptoms after theco-peritoneal shunt insertion.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Impact of Ketamine On Depressive Symptoms In Patients Undergoing Lumbo-peritoneal Shunt Insertion. A Randomized Double-blind Controlled Trial.
Anticipated Study Start Date :
Sep 29, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Group A

50-ml volume of normal saline

Drug: normal Saline
50-ml Saline

Active Comparator: Group B

50-ml volumes, and the ketamine concentration is 1 mg/ml

Drug: Ketamine
50-ml volumes, and the ketamine concentration is 1 mg/ml
Other Names:
  • katalar
  • Outcome Measures

    Primary Outcome Measures

    1. the rate of response to treating postoperative depression [at 3 postoperative days]

      defined as a relative reduction of more than 50% from the baseline 10-item MADRS score

    Secondary Outcome Measures

    1. The remission rate [at 1, 2, 5, and 7 days after the administration of ketamine.]

      defined as an absolute value of MADRS score of no more than 10

    2. The incidence of severe pain [within the first 48 hours postoperatively]

      From 0 to 10 (0 no pain , 10 very sever pain)

    3. The quality of life [within 7 days postoperatively]

      a scale ranging from 100-0, where 100 is labeled 'Perfect quality of life,' and 0 is labeled 'Might as well be dead'.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 44 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • patients of both sex

    • with an age range from 20 to 44 years old

    • having moderate to severe depressive symptoms

    • an expected hospital stay of no less than 7 days

    Exclusion Criteria:
    • history of epilepsy

    • major depressive disorder patients

    • drug abuse

    • history of allergy to the research drug

    • heart rate > 120 beats per minute

    • systolic blood pressure > 180 mmHg

    • heart failure

    • renal or liver dysfunction

    • patients who cannot cooperate to complete psychiatric assessments

    • pregnant or breast-feeding women

    • patients who refuse to sign informed consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Banha faculity of medicine Banha Elqalyoubea Egypt 13511

    Sponsors and Collaborators

    • Benha University

    Investigators

    • Principal Investigator: Fatma Ah Abdelfatah, MD, banha faculity of medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fatma Ahmed Abdel Fatah, lecturer, Benha University
    ClinicalTrials.gov Identifier:
    NCT06060210
    Other Study ID Numbers:
    • RC 12-9-2023
    First Posted:
    Sep 29, 2023
    Last Update Posted:
    Sep 29, 2023
    Last Verified:
    Sep 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Fatma Ahmed Abdel Fatah, lecturer, Benha University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 29, 2023