- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07816003
Machine Learning Prediction of Spinal Anaesthesia Block Duration
13 september 2026 uppdaterad av: SalahEldin Ahmed Abdelaziz Ahmed, Specialized Medical Center (SMC)
Artificial Intelligence-Based Prediction of Sensory and Motor Block Duration Following Spinal Anaesthesia: A Prospective Observational Prediction Model Development Study
The duration of sensory and motor block after spinal anaesthesia varies widely between patients given the same dose of local anaesthetic.
Much of this variability is explained by differences in lumbosacral cerebrospinal fluid volume, which cannot be measured routinely in clinical practice but is related to simple body measurements such as abdominal circumference and vertebral column length.
This prospective observational study will develop and internally validate prediction models for the duration of sensory and motor block following spinal anaesthesia in adults undergoing elective surgery.
Preoperative clinical and anthropometric variables will be recorded, and block regression will be assessed serially after intrathecal injection.
Machine learning methods (lasso regression, ridge regression, random forest, extreme gradient boosting, and support vector regression) will be developed and compared against multivariable linear regression as the reference model.
The aim is a practical tool that helps anaesthetists anticipate how long a spinal block will last in an individual patient, supporting decisions about case scheduling, supplementation, and discharge planning.
Studieöversikt
Status
Har inte rekryterat ännu
Betingelser
Detaljerad beskrivning
Background.
Spinal anaesthesia produces block of unpredictable duration.
Cerebrospinal fluid volume in the lumbosacral region is the dominant determinant of block spread and regression, and correlates inversely with abdominal circumference and directly with vertebral column length.
Existing single-variable rules perform poorly, and no validated multivariable model is in routine clinical use.
Objectives.
The primary objective is to develop and internally validate models predicting the duration of sensory block and the duration of motor block after single-shot spinal anaesthesia.
The secondary objective is to compare the predictive performance of machine learning approaches with conventional multivariable linear regression.
Design.
Single-centre prospective observational cohort study.
No study-directed intervention is applied; anaesthetic technique, drug, and dose are determined by the attending anaesthetist according to routine practice and are recorded as candidate predictors.
Assessments.
Sensory block level is assessed bilaterally by pinprick with a 25-gauge needle along the mid-clavicular line, over dermatomes T4 to S1. Motor block is assessed using the modified Bromage scale (0-3).
Assessments are performed at fixed intervals from intrathecal injection until complete regression of sensory and motor block.
Candidate predictors.
Age, sex, height, weight, body mass index, abdominal circumference, vertebral column length, ASA physical status, local anaesthetic dose and baricity, and adjuvant use.
Sample size.
A target of 255 participants was derived using the Riley criteria for continuous-outcome prediction models (pmsampsize), assuming 9 candidate predictors, an outcome standard deviation of 40 minutes, anticipated R-squared of 0.35, shrinkage of at least 0.90, and a multiplicative margin of error of 1.10.
The four criteria yielded 183, 183, 234, and 246; the largest requirement of 246 was inflated by approximately 4 per cent for attrition.
Analysis.
Model development will use nested repeated 10-fold cross-validation with bootstrap optimism correction.
Performance will be reported as R-squared, root mean squared error, and mean absolute error, with calibration plots.
SHAP values will be used to describe predictor contributions.
Reporting will follow TRIPOD+AI.
Studietyp
Observationell
Inskrivning (Beräknad)
255
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Salaheldin A Abdelaziz Ahmed
- Telefonnummer: +966508818713
- E-post: saladin28.sa@gmail.com
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Nej
Testmetod
Icke-sannolikhetsprov
Studera befolkning
Consecutive adults scheduled for elective surgery under single-shot spinal anaesthesia at Specialized Medical Center, King Fahad campus, Riyadh.
Beskrivning
Inclusion Criteria:
- Adults scheduled for elective surgery under single-shot spinal anaesthesia
- ASA physical status I to III
- Written informed consent obtained
Exclusion Criteria:
- Contraindication to neuraxial anaesthesia (coagulopathy, local or systemic infection, raised intracranial pressure, patient refusal)
- Failed or incomplete block requiring conversion to general anaesthesia
- Repeated or top-up intrathecal injection
- Pregnancy
- Known spinal deformity or previous spine surgery
- Pre-existing neurological or neuromuscular disease affecting sensory or motor assessment
- Inability to cooperate with sensory and motor assessment
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Duration of sensory block
Tidsram: Up to 8 hours after intrathecal injection
|
Time from completion of intrathecal injection to regression of sensory block to the S1 dermatome, assessed bilaterally by pinprick with a 25-gauge needle along the mid-clavicular line
|
Up to 8 hours after intrathecal injection
|
|
Duration of motor block
Tidsram: Up to 8 hours after intrathecal injection
|
Time from completion of intrathecal injection to return to modified Bromage score 0 (full ability to flex knee and ankle)
|
Up to 8 hours after intrathecal injection
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Predictive performance of machine learning models
Tidsram: Through study completion, an average of 20 months
|
R-squared, root mean squared error, mean absolute error, and calibration slope for lasso regression, ridge regression, random forest, extreme gradient boosting, and support vector regression, each compared with multivariable linear regression as the reference model
|
Through study completion, an average of 20 months
|
|
Time to peak sensory block level
Tidsram: Up to 30 minutes after intrathecal injection
|
Time from intrathecal injection to the highest dermatomal level of sensory block, assessed by pinprick
|
Up to 30 minutes after intrathecal injection
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Huvudutredare: Salaheldin A abdelaziz Ahmed, Specialized Medical Center
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
1 december 2026
Primärt slutförande (Beräknad)
1 juli 2028
Avslutad studie (Beräknad)
1 september 2028
Studieregistreringsdatum
Först inskickad
7 september 2026
Först inskickad som uppfyllde QC-kriterierna
7 september 2026
Första postat (Faktisk)
11 september 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
15 september 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
13 september 2026
Senast verifierad
1 september 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- IRBSMC1-2026-0001
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
JA
IPD-planbeskrivning
De-identified individual participant data underlying published results, together with the data dictionary and model code, will be made available to researchers whose proposed use has been approved by an independent review committee.
Requests should be directed to the principal investigator.
Data will be available from 6 months to 36 months after publication of the primary results.
Tidsram för IPD-delning
Data will become available 6 months after publication of the primary results and will remain available for 36 months
Kriterier för IPD Sharing Access
Requests should be directed to the principal investigator.
Proposals will be reviewed by the principal investigator and the Specialized Medical Center Institutional Review Board.
Requesters must provide a methodologically sound proposal and sign a data access agreement.
IPD-delning som stöder informationstyp
- STUDY_PROTOCOL
- SAV
- ICF
- ANALYTIC_CODE
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
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