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Hip FracturesNCT04614181

Protein and Carbohydrate Loading in Elderly With Hip Fractures

A study testing Nestle Resource drink in people with Hip Fractures, run by University of Malaya at 1 site in Malaysia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Pre-operative carbohydrate and protein loading among older people with hip fractures could potentially influence patient outcomes. This mode of intervention has seen good outcomes in a general surgical setting as part of its enhanced recovery pathway. Read more about this study

Who is it for?
Ages 65 years and older
Conditions the study is for
Hip Fractures
What is being tested?
Nestle Resource drink
Could I receive a placebo?
No, everyone receives an active treatment
How many people
34 participants
Where
1 siteMalaysia
Study dates
4 Nov 2020to 30 Dec 2021
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • No healthy volunteers
  • Older adult

Who may be able to join

  • All patients planned for semi-emergency hip surgery (total arthroplasty, hemiarthroplasty, internal fixation)
  • Aged 65 years and above
  • ASA 1-3 (ASA Physical Status Classification System)

Who cannot join

  • Patients undergoing hip surgery of emergency nature (inadequate time for recruitment and pre-operative intervention)
  • Peri-prosthetic hip fracture and fracture due to underlying malignancy
  • Revision hip surgery
  • Participation in another nutritional program
  • Diabetes mellitus
  • Intolerance to carbohydrate drinks
  • Gastric reflux, risk of aspiration, dysphagia
  • Severe cognitive impairment and delirium

Trial locations and contacts

1 site in 1 country.

Malaysia1 site
  • Faculty of Medicine, University of Malaya

    Kuala Lumpur, 50603

Other trials in Malaysia

About this study

Official title: The Feasibility and Benefits of Pre-operative Whey-protein Infused Carbohydrate Loading in Elderly With Hip Fractures Undergoing Surgery: a Pilot Study

Pre-operative carbohydrate and protein loading among older people with hip fractures could potentially influence patient outcomes. This mode of intervention has seen good outcomes in a general surgical setting as part of its enhanced recovery pathway. However, its effectiveness and ease of implementation in a hip fracture setting is uncertain. This study aims to study the feasibility of protein and carbohydrate loading as part of hip fracture management compared to usual care.

Read the detailed description

INTRODUCTION AND BACKGROUND

Pre-operative carbohydrate loading is one of the many components of enhanced recovery after surgery (ERAS) protocol. It has been identified as one of the independent predictors among ERAS components to improve peri-operative well-being and reduce post-operative complications. While well-being is a subjective outcome, several surrogate outcomes have been used to quantify some of the aspects. These surrogate outcomes of well-being include post-operative nausea and vomiting, pain, and preservation of muscle strength.

Although the exact mechanism of how pre-operative carbohydrate loading improves these outcomes is unclear, there appears to be an anabolic effect by increasing insulin sensitivity, improving glucose control and reducing catabolism. Patients in anabolic state undergo less post-operative nitrogen and protein loss, which translates to preservation of muscle strength. Carbohydrate loading keeps the body in a fed state during the fasting period before surgery. This abolishes the starvation effects which causes reduced insulin sensitivity commonly seen with conventional fasting practice. This is an independent predictor which prolongs length of hospital stay, preservation of muscle mass and handgrip strength post-operatively.

While most studies have demonstrated benefits of carbohydrate loading in patients undergoing abdominal surgeries, the number of studies conducted in the orthopedic hip fracture population are limited. In addition, there may also be barriers to introducing a new protocol with carbohydrate loading to replace the existing conventional fasting practice. Studies showed diverse feasibility in terms of implementation, which seemed to be multifactorial. More studies are therefore required to identify the factors promoting or impeding such a practice in respective centres. Given that a significant number of the hip fracture population are malnourished elderly who may benefit from this intervention, the gap in literature in this population deserves a thorough attention.

The University Malaya Medical Centre is a tertiary hospital with an average of 200 hip fracture cases annually. To date, these cases are subjected to conventional fasting starting from midnight. They are usually fasted up to extended hours, putting them in a starved state before surgery. It is therefore the great interest of the current multidisciplinary teams involved in the clinical care of hip fracture patients to introduce carbohydrate loading as part of the fasting practice. This study aims to introduce the concept and assess the feasibility of such a practice. The results from this pilot study may be used to revolutionize the fasting practice in our hospital.

OBJECTIVE

Primary objective

  1. To study the feasibility of implementing pre-operative carbohydrate loading in patients undergoing hip surgery
  2. To study the safety of pre-operative carbohydrate loading in patients undergoing hip surgery

Secondary objective

  1. To evaluate the effect of pre-operative carbohydrate loading among patients undergoing hip fracture surgery

METHODS

This is a pilot study to collect data on feasibility of implementing carbohydrate loading before orthopaedic hip fracture surgery. It is also an open labelled, randomized controlled study to identify correlation between pre-operative carbohydrate loading and surrogate outcomes of well-being. A computer generated randomization method will be used to allocate participants to each arm (intervention vs control) on a 1:1 ratio basis. The randomization allocation will be revealed after consent and baseline assessment.

The amount of carbohydrate load required to induce an effect must be enough to shift the body from a fasted to a fed state. A 50g oral carbohydrate ingestion has been shown to stimulate insulin release resembling post-prandial state. Therefore, the ERAS society recommendation is based on the following dose: a loading dose of 100g carbohydrate the day before surgery (as glycogen store) followed by a 50g dose 2 hours before surgery (to keep patients in a fed state).

In our study, the intervention group will receive the carbohydrate beverage (Nestle RESOURCE). Each serving is 237ml containing 53.6g of carbohydrate and 9g of protein. Intervention group will consume two servings of the carbohydrate beverage (53.6g each, total of approximately 100g) on the day before surgery and one serving 6 hours prior to scheduled surgery time. The control group will receive usual hip fracture care as determined by the clinical team.

SAMPLE SIZE

For this pilot study, a sample size of 40 is targeted. 20 will be randomized to the intervention group receiving the supplement drink, while 20 will be randomized to the control group who will not be receiving any supplements. No formal sample size calculation was used. One of the objectives of this feasibility study is to provide estimates of recruitment and retention rates for a larger study. The number of participants for this study will be determined by resources and the recruitment period.

ANALYSIS

Baseline demographic data will be presented as mean ± SEM. Feasibility outcomes will be reported as numbers and percentages. Descriptive statistics (mean, standard deviation, and median for continuous variables; frequencies and percentages for categorical variables) will be calculated separately by group. For the group comparison, appropriate tests based on their distribution will be performed.

Conditions
Hip Fractures
Being tested
Nestle Resource drink, Usual care
Medical subject headings
Hip Fractures

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nestle Resource drinkDietary supplement

    Beverage (Nestle RESOURCE). Each serving is 237ml containing 53.6g of carbohydrate and 9g of protein. Intervention group will consume two servings of the carbohydrate beverage (53.6g each, total of approximately 100g) on the day before surgery and one serving up to 6 hours prior to scheduled surgery time.

  • Usual careOther

    Usual fracture care as determined by clinical team

Study groups in NCT04614181
Study groupRoleWhat they receive
Carbohydrate and protein loadingExperimentalNestle Resource drink
Receives: Dietary Supplement: Nestle Resource drink
Usual careActive comparatorUsual fracture care as determined by clinical team
Receives: Other: Usual care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The number of participants recruitment

    How many participants willing to be recruited, screening to recruitment rate

    Measured: 6 months

  2. The number of participants that adhered to nutritional loading

    How many participants adhered to the the total treatment drinks

    Measured: 6 months

  3. The attrition rate of participants recruited into the study

    How many participants dropped out or had missing data

    Measured: 6 months

  4. Safety profile: How many participants had an adverse reaction

    How many participants had an adverse reaction

    Measured: 6 months

Secondary outcomes (5)
  1. Prevalence of post-operative nausea and/or vomiting

    Number of participants with post-operative nausea and/or vomiting

    Measured: 6 months

  2. Severity of post-operative pain

    Resting and dynamic pain assessed at 48-72 hours

    Measured: 6 months

  3. Length of stay

    Inpatient length of acute hospital stay

    Measured: 6 months

  4. Change in muscle strength

    Difference of hand grip strength and anthropometric measurements pre- and post-operatively

    Measured: 6 months

  5. Prevalence of post-operative complications

    Number of participants that developed complications after surgery (infection, cardiovascular, kidney injury, stroke, thromboembolism, pressure ulcer)

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Nov 2020
  2. Study start4 Nov 2020
  3. Primary completion29 Jun 2021
  4. Study completion30 Dec 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
34 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04614181
Sponsor's protocol ID
2020629-8833 56379
Status last verified
May 2022
First submitted
20 Oct 2020
Last updated
20 May 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Yap KS, Loh PS, Foong YX, Mok CZ, Ong T, Khor HM. A feasibility study on preoperative carbohydrate loading in older patients undergoing hip fracture surgery. BMC Geriatr. 2024 May 6;24(1):401. doi: 10.1186/s12877-024-04958-7.

    PubMed 38711010

Questions about this trial

What is this clinical trial studying?

A study testing Nestle Resource drink in people with Hip Fractures, run by University of Malaya at 1 site in Malaysia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 May 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Malaysia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The number of participants recruitment (time frame: 6 months). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04614181, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 May 2022.

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